Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → (S)-(+)-Glycidyl butyrate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | Glycidyl butyrate | HCID 137606 | — |
| 반응물 | (-)-Benzyl (R)-glycidyl ether | HCID 159746 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-(+)-Glycidyl butyrate | HCID 6999819 | 44% |
반응 단계
Using the (R,R)-(salen)Co(II) precatalyst of 1 (91 mg, 0.15 mmol, 0.005equiv), (+/−)-glycidyl butyrate (4.32 g, 30.0 mmol), AcOH (32 mL, 0.6 mnmol, 0.02 equiv), 0.3 mL THF, and H2O (297 mL, 16.5 mmol, 0.55 equiv) and a procedure analogous to the one outlined for 5b, (S)-glycidyl butyrate 5d (1.90 g, 13.2 mmol, 44%) was obtained as a clear oil by vacuum distillation of the reaction mixture (30° C., 0.5 torr). The product was determined to be >99% ee by conversion to and analysis of the 2-napthylsulfide (obtained by ring opening with 2-napthalenethiol in methanol using 1 equiv TEA at 0° C.; Chiralcel OD, 97:3 hexanes:EtOH, 1 mL/min, 260 mn).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06800766B2 |
| 출처 데이터셋 | uspto-grants-2004_10 |
| ORD ID | ord-6d85519c2fdc4c0d8339146ac19faa4b |
| 출처 메모 | uspto-grants-2004_10 |