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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453106생성일: 2026년 10월 26일

Sodium borohydride → [3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanol

https://huagongshe.com/reaction/453106

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl esterHCID 59549532—
용매EthanolHCID 702—
생성물[3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanolHCID 5954952230%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492414B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-903234933b774e1e8e71b928d59b05de
출처 메모uspto-grants-2013_07