참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Propanoic acid, 2,2,3,3,3-pentafluoro-, ethyl ester | HCID 67928 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 반응물 | HCID 178472209 | HCID 178472209 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | HCID 178469142 | HCID 178469142 | 30.7% |
반응 단계
To a -78° C. solution of LDA (0.10 mol), prepared from 0.10 mol of n-BuLi and 14 ml (0.10 mol) of diisopropylamine in 70 ml ether was added a solution of 10.0 g (0.042 mol) of product of Example 34 in 20 ml of ether slowly to maintain a temperature below -60° C. After stirring for 30 minutes, the reaction mixture was treated with 21 ml (0.042 mol) of ethyl pentafluoropropionate. After stirring at -78° C. for 15 minutes, the reaction mixture was warmed to 10° C. in 0.5 hour and poured into 100 ml of water, and extracted with ether. The ether extract was extracted with 10% K2CO3. The combined aqueous layer and K2CO3 extract was acidified with concentrated HCl to give 4.73 g (29.5%) of beige solid; mp 115°-117° C. (dec). A 2.73 g (0.00709 mol) of the solid was heated in a kugelrohr pot at 130° C. for 0.5 hour. The distillate and residue were combined and dissolved in ether. The ether solution was dried (CaSO4) and concentrated to give 2.0 g (76.9%) of product as a solid; mp 36°-38° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04655816 |
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| 출처 데이터셋 | uspto-grants-1987_04 |
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| ORD ID | ord-b132052dda1a42b084f6d6e2749934bd |
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| 출처 메모 | uspto-grants-1987_04 |
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