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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1987568생성일: 2026년 10월 25일

Lithium borohydride → 4-chloro-N-[(1S)-4,4,4-trifluoro-1-hydroxymethyl-2-(2,2,2-trifluoroethyl)-butyl]benzenesulfonamide

https://huagongshe.com/reaction/1987568

반응식

참여 물질

역할이름HCID투입량
반응물Lithium borohydrideHCID 4148881—
반응물(2S)-2-(4-chloro-benzenesulfonylamino)-5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)pentanoic acid methyl esterHCID 25112113—
용매TetrahydrofuranHCID 8028—
생성물4-chloro-N-[(1S)-4,4,4-trifluoro-1-hydroxymethyl-2-(2,2,2-trifluoroethyl)-butyl]benzenesulfonamideHCID 57529272177.2%

반응 단계

A solution of (2S)-2-(4-chloro-benzenesulfonylamino)-5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)-pentanoic acid methyl ester (130 mg, 0.30 mmol) in THF (5 mL) was treated with LiBH4 (2M THF, 0.3 mL, 0.58 mmol) for 18 hours at 25° C. The reaction was carefully quenched by the addition of 2M HCl and the organic solvent removed in vacuo. The aqueous layer was extracted with EtOAc (2×10 mL). The organic layers were combined, dried over Na2SO4 and evaporated to afford a crude oil which was purified by flash chromatography eluting with 30:70 EtOAc:hexanes to provide the title compound as a white solid (220 mg) in 63% yield. Mass Spectrum (−ESI): 412.0 [M−H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07550629B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-7dcf141d5d81439eb6045f6f1aebebda
출처 메모uspto-grants-2009_06