참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formic Acid | HCID 284 | — |
| 반응물 | P-Cymene | HCID 7463 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethyl 2-chloro-3-oxo-4-phenylbutyrate | HCID 11601176 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chlorobenzene | HCID 7964 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | ethyl (3R)-2-chloro-3-hydroxy-4-phenylbutyrate | HCID 59203390 | 107.1% |
반응 단계
Ethyl 2-chloro-3-oxo-4-phenylbutyrate (180 mg, 0.7 mmol) and RuCl[(S,S)-TsDPEN])p-cymene) complex (10 mg, 2 mol %) were mixed, and the mixture was dissolved in chlorobenzene (1 ml). A chlorobenzene solution (1 ml) of triethylamine (374 mg, 5 equivalents) was added, and then a chlorobenzene solution (1 ml) of formic acid (102 mg, 3 equivalents) was gradually added dropwise. After the mixture was stirred at 40° C. for 3 hours, water (4 ml) was added. Ethyl acetate (10 ml) was added for extraction, and the organic layer was concentrated under reduced pressure to obtain the title compound as a brown oil (182 mg, yield: 100%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07834190B2 |
|---|
| 출처 데이터셋 | uspto-grants-2010_11 |
|---|
| ORD ID | ord-0fb06840647044cc93f881a40e5455f8 |
|---|
| 출처 메모 | uspto-grants-2010_11 |
|---|