Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Acetylbutyric acid → Pentafluorophenyl 5-oxohexanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Acetylbutyric acid | HCID 18407 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Pentafluorophenyl 5-oxohexanoate | HCID 86609189 | 79.3% |
반응 단계
5-Oxohexanoic acid (2.6 g; 20 mmol) was dissolved in CH2Cl2 (50 mL). N,N-Diisopropylethylamine (10.4 mL, 60 mmol) was added followed by pentafluorophenyl trifluoroacetate (3.61 mL; 21 mmol). The reaction mixture was kept at room temperature for 1 hour and evaporated. The residue was resuspended in EtOAc:Hexanes (1:1) and loaded on a silica gel column (5×20 cm) equilibrated and developed with the same mixture. Fractions containing the product (14) (Rf ˜0.7) were pooled and concentrated to give 4.7 g (79%) of yellowish oil after drying in vacuum. 1H NMR (CDCl3) δ 2.05 (m, 2H), 2.18 (s, 3H), 2.61 (t, 2H), 2.74 (t, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08030460B2 |
| 출처 데이터셋 | uspto-grants-2011_10 |
| ORD ID | ord-2198ed722c8541519be28b40df71a586 |
| 출처 메모 | uspto-grants-2011_10 |