Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium borohydride → [3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester | HCID 59549532 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | [3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanol | HCID 59549522 | 30% |
반응 단계
To a solution of 3-(4-benzyloxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.20 g, 0.59 mmol) in EtOH (20 ml) was added sodium borohydride (0.44 g, 1.17 mmol) portion wise and the resulting reaction mixture was stirred at room temperature for 2 h. After the completion of the reaction (TLC monitoring), the reaction mass was cooled to 0° C., quenched it with 5 ml of water and concentrated under vacuum. Added 75 ml water and extracted with ethyl acetate (3×30 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum. The crude residue was purified over silica gel (100-200 M, 30% EtOAc-Hexane) to get the desired product (0.052 g, 30%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08492414B2 |
| 출처 데이터셋 | uspto-grants-2013_07 |
| ORD ID | ord-903234933b774e1e8e71b928d59b05de |
| 출처 메모 | uspto-grants-2013_07 |