GB553305A - Improvements in and relating to the production of unsaturated ketones and their related keto alcohols - Google Patents
Improvements in and relating to the production of unsaturated ketones and their related keto alcoholsInfo
- Publication number
- GB553305A GB553305A GB1171441A GB1171441A GB553305A GB 553305 A GB553305 A GB 553305A GB 1171441 A GB1171441 A GB 1171441A GB 1171441 A GB1171441 A GB 1171441A GB 553305 A GB553305 A GB 553305A
- Authority
- GB
- United Kingdom
- Prior art keywords
- paraformaldehyde
- parts
- acetone
- weight
- product
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/17—Saturated compounds containing keto groups bound to acyclic carbon atoms containing hydroxy groups
-
- 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
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/65—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
- C07C45/66—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups by dehydration
-
- 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
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/75—Reactions with formaldehyde
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
553,305. Keto-butanol derivatives. COLMORE ADHESIVES, Ltd., and WHITE, T. Sept. 12, 1941, No. 11714. [Class 2 (iii)] 3-Ketobutanol is prepared by reacting 40 parts by weight of paraformaldehyde with 300 parts by weight of acetone at a pH of between 7.5 and 9.0. 2-Methyl-3-ketobutanol is similarly obtained using 30 parts of paraformaldehyde to 200 parts by weight of methylethylketone. The ketoalcohols, which are preferably purified by distillation in the presence of a high boiling ester, e.g. dibutylphthalate, yield the corresponding unsaturated ketones by dehydration with, e.g. sulphuric, phosphoric or oxalic acid, alkalibisulphates, calcium chloride, quicklime, halogens or anhydrous copper sulphate. In examples : (1) acetone and paraformaldehyde are refluxed with methylalcoholic potash and the product distilled with dibutylphthalate after neutralization ; (2) the product obtained in example (1) is distilled with concentrated phosphoric acid and the crude methylvinylketone freed from acetone by fractional distillation after removing water by heating with acetic anhydride ; (3) methylethylketone is similarly treated with paraformaldehyde and methyl isopropenylketone obtained by dehydrating the product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1171441A GB553305A (en) | 1941-09-12 | 1941-09-12 | Improvements in and relating to the production of unsaturated ketones and their related keto alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1171441A GB553305A (en) | 1941-09-12 | 1941-09-12 | Improvements in and relating to the production of unsaturated ketones and their related keto alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB553305A true GB553305A (en) | 1943-05-17 |
Family
ID=9991337
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1171441A Expired GB553305A (en) | 1941-09-12 | 1941-09-12 | Improvements in and relating to the production of unsaturated ketones and their related keto alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB553305A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6322642B1 (en) | 1998-07-21 | 2001-11-27 | Creusot Loire Industrie | Process and steel for the manufacture of a pressure vessel working in the presence hydrogen sulfide |
-
1941
- 1941-09-12 GB GB1171441A patent/GB553305A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6322642B1 (en) | 1998-07-21 | 2001-11-27 | Creusot Loire Industrie | Process and steel for the manufacture of a pressure vessel working in the presence hydrogen sulfide |
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