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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266094생성일: 2026년 10월 27일

Sodium borohydride → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolemethanol

https://huagongshe.com/reaction/266094

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물[2-Benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl)methanoneHCID 9842862—
용매MethanolHCID 887—
생성물alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolemethanolHCID 18930333—

반응 조건

온도0 °C

반응 단계

Dissolve [2-benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone (3.0 g, 7.88 mmol) in methanol (150 mL) and cool to 0° C. Add sodium borohydride (597 mg, 15.77 mmol) and stir for 1.5 hours, adding additional sodium borohydride after 30 minutes. Evaporate the solvent in vacuo and partition the residue between water and methylene chloride. Separate the organic phase, wash with saturated sodium chloride, dry (MgSO4) and evaporate the solvent in vacuo. Purify by recrystallization (ethyl acetate) to give the title compound as white fluffy crystals; mp 127°-129° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650416
출처 데이터셋uspto-grants-1997_07
ORD IDord-e3d0f09abc84486991f02f7687bec246
출처 메모uspto-grants-1997_07