CN1069963A - The method of enol and alkene ether preparing unsaturated carbonyl compound by reaction - Google Patents
The method of enol and alkene ether preparing unsaturated carbonyl compound by reaction Download PDFInfo
- Publication number
- CN1069963A CN1069963A CN 92109831 CN92109831A CN1069963A CN 1069963 A CN1069963 A CN 1069963A CN 92109831 CN92109831 CN 92109831 CN 92109831 A CN92109831 A CN 92109831A CN 1069963 A CN1069963 A CN 1069963A
- Authority
- CN
- China
- Prior art keywords
- reaction
- enol
- alkene ether
- temperature
- unsaturated carbonyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/513—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an etherified hydroxyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention provides a kind of method by enol and alkene ether prepared in reaction γ, the unsaturated aldehyde ketone of σ.Present method is that reaction is divided into two stages, and the fs temperature is low, and the time is long; Subordinate phase temperature height, the time is short, obtains beyond thought effect, and yield improves 30%, and has changed order of addition(of ingredients), and is easy and simple to handle, is suitable for suitability for industrialized production.
Description
The invention belongs to the reaction of enol and alkene ether and produce the method for γ, the unsaturated aldehyde ketone of σ.
Enol and alkene ether prepared in reaction γ, the unsaturated aldehyde ketone of σ have research and report external morning, and its structural formula is as follows:
R2 R3 R4 R5
R1 is alkyl or H in the formula, also can be oxy radical, and R2, R4, R5 are alkyl or H, lower paraffin hydrocarbons, alkene, naphthenic hydrocarbon, cycloolefin and aromatic hydrocarbon.Above-mentioned beta-unsaturated carbonyl compounds is the important intermediate of synthesise vitamins A, vitamin-E, but also synthetic perfume.
Belg patent 634,738, and same Patent US Patent 3,574,715 has narrated enol and alkene ether prepared in reaction γ, σ beta-unsaturated carbonyl compounds, is 125 ℃ of fixed temperatures, reacts yield about 60% 16 hours.Above-mentioned patent is that (0-10 ℃) adds alkene ether with catalyzer at low temperatures, adds solvent, enol again, and a large amount of refrigerants of charging process consumption are uneconomical like this.
The objective of the invention is to make the reaction of enol and alkene ether to generate the unsaturated aldehyde ketone yield of γ, σ and improve, change charging process, earlier enol is added reactor, can save the energy in ambient operation, easy and simple to handle, be suitable for the preparation of industrialization beta-unsaturated carbonyl compounds.
The object of the present invention is achieved like this: enol and alkene ether reaction generation γ, the reaction of σ unsaturated aldehyde ketone compound are divided into two stages, earlier enol is added reactor in room temperature, add catalyzer, back adding organic solvent stirs, add alkene ether again, react fs temperature 80-170 ℃, reacted 8-40 hour, heat up then; Subordinate phase temperature of reaction T2 is than high 50-100 ℃ of fs temperature of reaction T1, and subordinate phase reaction times t2 is 1/100 to 1/7 of reaction times fs t1.
The present invention generates the reaction mechanism of γ, the unsaturated aldehyde ketone of σ according to enol and alkene ether reaction, adopted unique zone heating method, because enol and alkene ether reaction fs have generated acetal in the presence of an acidic catalyst, continue reaction with this understanding and take off a part alcohol.Fs optimum reacting time 16-30 hour, can finish for 110-150 ℃.The two keys of subordinate phase carry out transposition, and isomerization reaction needs high temperature, and the time is short.Go out above-mentioned two sections heating means by test and Selection, obtain beyond thought effect.The unsaturated aldehyde ketone yield of γ, σ that generates has improved 30%, need not be freezing when reinforced, and save energy, easy and simple to handle, be suitable for suitability for industrialized production.
The enol of reaction usefulness has: 3-methyl-1-butene-3-alcohol, 2,3-dimethyl-1-butylene-3-alcohol, 3-Methyl-1-pentene-3-alcohol, 3,7-dimethyl-1,6-diene triol (Linalool), 3,7,11-trimethylammonium-1,6,100 two carbon triolefin-3-alcohol (nerolidol), different vegetable alcohol, 3,7-dimethyl-7-methoxyl group-1-butylene triol (that alcohol of methoxy methyl); Alkene ether commonly used has: isopropyl methyl ether, 2-oxyethyl group-1-butylene base ether, 2-oxyethyl group-3-or alkene ether, 2-oxyethyl group-2, and 5-hexadienyl ether, 1-tetrahydrobenzene butyl ether, catalysts adopts acid catalyst, as H
3PO
4, or tosic acid, also useful hydrogen sulfate first, action solvent is generally used hydrocarbon, hexanaphthene, normal hexane, octane-iso, benzene, toluene and their mixture, sherwood oil, flux wet goods.
In order to understand the present invention, as follows for embodiment:
Embodiment 1:
In the 100ml autoclave, add 15 grams 3,7-dimethyl-1,6-octadiene-3-alcohol (Linalool) adds 0.1 gram 85%H
3PO
4, add 6-7 gram 120# solvent oil, cover the high pressure kettle cover, stirred 2-5 minute, stop to stir, be evacuated to 260mmHg, logical N
2Gas three times and so forth, adds the different propylene methyl ether of 30 grams, feeding N to normal pressure
2Gas lift is depressed into 2 kg/cm, opens stirring, is rapidly heated 120 ℃, reacts 30 hours, improves temperature then fast to 180 ℃ of interior temperature, reacts 15 hours.Cooling, exhaust move into matrass with material, add triethylamine and are neutralized to PH=7.The air distillation foreshot is different propylene methyl ether, and middle fraction is a Propanal dimethyl acetal, and after cut is the 120# solvent oil.The cold slightly back underpressure distillation of remaining material.＜68 ℃/2mmHg is a foreshot, can be inserted in down batch reaction liquid.68-75 ℃/2mmHg is positive fraction, geranyl acetone, and purity 〉=95%, yield 92%(is to Linalool).
Embodiment 2
In the 100ml autoclave, add 20 grams 3,7-11-trimethylammonium-1,6,10-12 carbon triolefin-3-alcohol (nerolidol), 0.15 gram 85%H
3PO
4, 8-9 gram 120# solvent oil covers the high pressure kettle cover, stirs 2-3 minute, stops to stir, and is evacuated to 260mmHg, logical N
2Gas three times and so forth, adds different propylene methyl ether, feeding N to normal pressure
2Gas lift is depressed into 2 kg/cm, starts stirring, and temperature is 145 ℃ in rising to fast, and reaction is 36 hours under this temperature, and temperature is 195 ℃ in rising to fast then, reacts 4 hours.Cooling, exhaust move into matrass with material, add triethylamine and are neutralized to PH=7.Air distillation, foreshot are different propylene methyl ether, and middle fraction is a Propanal dimethyl acetal, and after cut is the 120# solvent oil.The cold slightly back underpressure distillation of remaining material.＜120 ℃/0.5mmHg is a foreshot, can be inserted in down batch reaction liquid.120-165 ℃/0.5mmHg is positive fraction farnesyl acetone, purity 〉=92%, yield 83-86%(is to nerolidol).
Claims (2)
1, the reaction of a kind of enol and alkene ether generates the method for γ, the unsaturated aldehyde ketone of σ, it is characterized in that enol and alkene ether reaction generation γ, the reaction of σ unsaturated aldehyde ketone compound are divided into two stages, earlier enol is added reactor in room temperature, add catalyzer, add organic solvent after stirring, add alkene ether again, react fs temperature 80-170 ℃, reacted 8-40 hour, and heated up then; Subordinate phase temperature of reaction T2 is than high 50-100 ℃ of fs temperature of reaction T1, and subordinate phase reaction times t2 is 1/100 to 1/7 of reaction times fs t1.
2, method according to claim 1, the best that it is characterized in that reacting the fs temperature is 110-150 ℃.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 92109831 CN1033577C (en) | 1992-08-18 | 1992-08-18 | Process for preparing unsaturated carbonyl compound by reaction of olefinic alcohol and enol ether |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 92109831 CN1033577C (en) | 1992-08-18 | 1992-08-18 | Process for preparing unsaturated carbonyl compound by reaction of olefinic alcohol and enol ether |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1069963A true CN1069963A (en) | 1993-03-17 |
| CN1033577C CN1033577C (en) | 1996-12-18 |
Family
ID=4944384
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 92109831 Expired - Fee Related CN1033577C (en) | 1992-08-18 | 1992-08-18 | Process for preparing unsaturated carbonyl compound by reaction of olefinic alcohol and enol ether |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1033577C (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102197014A (en) * | 2008-10-21 | 2011-09-21 | 帝斯曼知识产权资产管理有限公司 | Manufacture of gamma-delta-unsaturated ketones |
| US8875539B2 (en) | 2011-07-20 | 2014-11-04 | Lg Electronics Inc. | Refrigerator |
| CN108299171A (en) * | 2018-02-11 | 2018-07-20 | 浙江新和成股份有限公司 | A method of by 2-M3BOL synthesizing methyl heptenone |
-
1992
- 1992-08-18 CN CN 92109831 patent/CN1033577C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102197014A (en) * | 2008-10-21 | 2011-09-21 | 帝斯曼知识产权资产管理有限公司 | Manufacture of gamma-delta-unsaturated ketones |
| CN102197014B (en) * | 2008-10-21 | 2013-12-04 | 帝斯曼知识产权资产管理有限公司 | Manufacture of gamma-delta-unsaturated ketones |
| US8875539B2 (en) | 2011-07-20 | 2014-11-04 | Lg Electronics Inc. | Refrigerator |
| CN108299171A (en) * | 2018-02-11 | 2018-07-20 | 浙江新和成股份有限公司 | A method of by 2-M3BOL synthesizing methyl heptenone |
| CN108299171B (en) * | 2018-02-11 | 2021-03-16 | 浙江新和成股份有限公司 | Method for synthesizing methyl heptenone from 2-methyl-3-butene-2-ol |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1033577C (en) | 1996-12-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Okamura et al. | Cross-coupling of alkenyl, aryl or allylic selenides and grignard reagents catalyzed by nickel-phosphine complexes | |
| US6380437B1 (en) | Process for the preparation of unsaturated 4,5-allene ketones, 3,5-diene ketones and the corresponding saturated ketones | |
| CN112142592A (en) | Method for synthesizing acetate perfume | |
| CN1033577C (en) | Process for preparing unsaturated carbonyl compound by reaction of olefinic alcohol and enol ether | |
| US6133487A (en) | Process for the oxidation of aromatic compounds to hydroxyaromatic compounds | |
| EP0760355B1 (en) | Process for the preparation of cyclopentadienyl derivatives | |
| WO1997032836A1 (en) | Process for producing unsaturated alcohols | |
| CA1146573A (en) | Production of butyrolactone | |
| CA1299189C (en) | (phenylethenyl)phenylpropionic acid and its ester, and method for producing (benzoylphenyl)propionic acid or its ester | |
| Tabuchi et al. | Palladium-catalyzed reaction of propargylic acetates with carbonyl compounds by SmI2 | |
| US4472313A (en) | Cyclopropanation of olefins | |
| EP0018164B1 (en) | Production of tetrahydrofuran | |
| Ohshima et al. | A convenient method for the preparation of γ-ketosulfides from thioacetals | |
| CN116041299B (en) | Synthesis method of nerol | |
| Grieco et al. | Phenylthioacetic acid dianion: latent vinyl, oxiranyl, and acyl carbanion equivalents | |
| CA1147747A (en) | Process for preparing alpha-naphthol esters of aliphatic carboxylic acids | |
| Kabalka et al. | Boron Triiodide-NN-diethylaniline Complex: A New Reagent for Cleaving Esters | |
| GB1604057A (en) | Cyclohexene derivatives useful in carotinoid synthesis and their preparation | |
| US3395160A (en) | Process for producing substituted benzoquinones and hydroquinones | |
| Yang et al. | Novel carbon catalysis: oxidation in basic solution | |
| Antonsson et al. | Selective formation of substituted cyclopentane derivatives from hexa-1, 5-dienes via oxidative cyclization in the presence of Pd (OAc) 2–MnO 2–benzoquinone as catalyst | |
| CA1338626C (en) | Processes for preparing alkylene and dialkyl ketals and alkyl alpha-enol ethers of alpha-acetyl cinnamic acids or esters thereof | |
| US4529825A (en) | Method for the preparation of a trans-isomer of ethylenically unsaturated organic compounds | |
| CA1179375A (en) | Process for improving ethylene glycol | |
| JPS6139294B2 (en) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |