JPH037651B2 - - Google Patents
Info
- Publication number
- JPH037651B2 JPH037651B2 JP19279484A JP19279484A JPH037651B2 JP H037651 B2 JPH037651 B2 JP H037651B2 JP 19279484 A JP19279484 A JP 19279484A JP 19279484 A JP19279484 A JP 19279484A JP H037651 B2 JPH037651 B2 JP H037651B2
- Authority
- JP
- Japan
- Prior art keywords
- acid ester
- heptafluoroisobutenyl
- alcohol
- ether
- alkyl ether
- 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
- -1 hexafluoroisobutanoic acid ester Chemical class 0.000 claims description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 150000005215 alkyl ethers Chemical class 0.000 description 4
- 238000005796 dehydrofluorination reaction Methods 0.000 description 4
- FSDLLONBRLBIBL-UHFFFAOYSA-N 1,3,3,3-tetrafluoro-1-methoxy-2-(trifluoromethyl)prop-1-ene Chemical compound COC(F)=C(C(F)(F)F)C(F)(F)F FSDLLONBRLBIBL-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BSZWZZSFVRISOG-UHFFFAOYSA-N 1-ethoxy-1,3,3,3-tetrafluoro-2-(trifluoromethyl)prop-1-ene Chemical compound CCOC(F)=C(C(F)(F)F)C(F)(F)F BSZWZZSFVRISOG-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- JGGBVFLRNNDHCM-UHFFFAOYSA-N methyl 3,3,3-trifluoro-2-(trifluoromethyl)propanoate Chemical compound COC(=O)C(C(F)(F)F)C(F)(F)F JGGBVFLRNNDHCM-UHFFFAOYSA-N 0.000 description 2
- DAFIBNSJXIGBQB-UHFFFAOYSA-N perfluoroisobutene Chemical compound FC(F)=C(C(F)(F)F)C(F)(F)F DAFIBNSJXIGBQB-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- LCRBBUPAHHPMMY-UHFFFAOYSA-N 1,3,3,3-tetrafluoro-1-[1,3,3,3-tetrafluoro-2-(trifluoromethyl)prop-1-enoxy]-2-(trifluoromethyl)prop-1-ene Chemical compound FC(F)(F)C(C(F)(F)F)=C(F)OC(F)=C(C(F)(F)F)C(F)(F)F LCRBBUPAHHPMMY-UHFFFAOYSA-N 0.000 description 1
- AQHKYFLVHBIQMS-UHFFFAOYSA-N 2-[difluoro(methoxy)methyl]-1,1,1,3,3,3-hexafluoropropane Chemical compound COC(F)(F)C(C(F)(F)F)C(F)(F)F AQHKYFLVHBIQMS-UHFFFAOYSA-N 0.000 description 1
- RAEAYTICAPHWJW-UHFFFAOYSA-N 3,3,3-trifluoro-2-(trifluoromethyl)propanoic acid Chemical compound OC(=O)C(C(F)(F)F)C(F)(F)F RAEAYTICAPHWJW-UHFFFAOYSA-N 0.000 description 1
- KMTDMTZBNYGUNX-UHFFFAOYSA-N 4-methylbenzyl alcohol Chemical compound CC1=CC=C(CO)C=C1 KMTDMTZBNYGUNX-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- HOSPDBQHPFVHEZ-UHFFFAOYSA-N ethyl 3,3,3-trifluoro-2-(trifluoromethyl)propanoate Chemical compound CCOC(=O)C(C(F)(F)F)C(F)(F)F HOSPDBQHPFVHEZ-UHFFFAOYSA-N 0.000 description 1
- 238000007701 flash-distillation Methods 0.000 description 1
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
- 239000002920 hazardous waste Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19279484A JPS6169745A (ja) | 1984-09-14 | 1984-09-14 | ヘキサフルオロイソブタン酸エステルの製造法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19279484A JPS6169745A (ja) | 1984-09-14 | 1984-09-14 | ヘキサフルオロイソブタン酸エステルの製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6169745A JPS6169745A (ja) | 1986-04-10 |
| JPH037651B2 true JPH037651B2 (de) | 1991-02-04 |
Family
ID=16297099
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19279484A Granted JPS6169745A (ja) | 1984-09-14 | 1984-09-14 | ヘキサフルオロイソブタン酸エステルの製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6169745A (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3945147A1 (de) | 2020-07-28 | 2022-02-02 | Novel Crystal Technology, Inc. | Vorrichtung und verfahren zur herstellung von einkristallen |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4739123A (en) * | 1985-10-21 | 1988-04-19 | Daiken Industries, Ltd. | Fluorine-containing compounds, and their preparation and use |
| US6023002A (en) * | 1998-01-26 | 2000-02-08 | 3M Innovative Properties Company | Process for preparing hydrofluoroethers |
| US6849194B2 (en) | 2000-11-17 | 2005-02-01 | Pcbu Services, Inc. | Methods for preparing ethers, ether compositions, fluoroether fire extinguishing systems, mixtures and methods |
| JP4883155B2 (ja) * | 2009-08-24 | 2012-02-22 | マックス株式会社 | 空気清浄機 |
-
1984
- 1984-09-14 JP JP19279484A patent/JPS6169745A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3945147A1 (de) | 2020-07-28 | 2022-02-02 | Novel Crystal Technology, Inc. | Vorrichtung und verfahren zur herstellung von einkristallen |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6169745A (ja) | 1986-04-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2526661B2 (ja) | フルオロアルキルビニル化合物の製造法 | |
| JPH037651B2 (de) | ||
| US4595541A (en) | Process for the preparation of trifluoroacetic anhydride | |
| JPH03106848A (ja) | α―フルオロアクリロイル誘導体の製造方法 | |
| JPH0332548B2 (de) | ||
| JP2001322955A (ja) | ２−ブロモ−３，３，３−トリフルオロプロペンの製造方法 | |
| JPH0585968A (ja) | ヒドロゲンペルフルオロアルカンの合成 | |
| JP3864997B2 (ja) | ２，４−オキサゾリジンジオン類の製造方法 | |
| JPH07112997B2 (ja) | ヘキサフルオロイソブタン酸の製造法 | |
| JPH0717660B2 (ja) | １，１―ジクロロ―１，２，２―トリメチル―２―フェニルジシランの製造方法 | |
| JPS6335534A (ja) | ヘプタフルオロイソブテニル低級アルキルエーテルの製造法 | |
| JPH0258269B2 (de) | ||
| JPS5835977B2 (ja) | ピバリン酸クロライドと芳香族カルボン酸クロライドの製造法 | |
| JPH0542418B2 (de) | ||
| JP2940560B2 (ja) | パーフルオロプロピオン酸フロリドの製造法 | |
| JP3149537B2 (ja) | １ｈ−ペルフルオロアルカンの製造法 | |
| JP3864648B2 (ja) | １，３−ビス（カルボキシアルキル）テトラアルキルジシロキサンの製造方法 | |
| JPS62106036A (ja) | ヘキサフルオロイソブテニルメチルエーテルの製造法 | |
| JPH10120674A (ja) | ２−メチル−３−（３，４−メチレンジオキシフェニル）アクリルアルデヒドの製法 | |
| JPH1095760A (ja) | シアノ酢酸エステルの製造法 | |
| JP4175738B2 (ja) | アルコキシプロピオン酸アルキルの製造方法 | |
| JPH1192413A (ja) | ２置換−１，３−インダンジオン誘導体の製造法 | |
| JPS62145043A (ja) | 新規なハロゲノテトラフルオロプロピオン酸、その製法およびその使用法 | |
| JPS5924142B2 (ja) | 酸アミドの製造方法 | |
| JPH1121281A (ja) | ２，４−オキサゾリジンジオンの製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |