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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677090생성일: 2026년 10월 26일

Tetrahydrofuran → (3R,5R)-3-((R)-1-hydroxyethyl)-5-(3,4,5-trifluorophenyl)morpholine-4-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1677090

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Benzyl chloroformateHCID 10387—
반응물Sodium BicarbonateHCID 516892—
반응물(R)-1-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]ethanolHCID 67374002—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물(3R,5R)-3-((R)-1-hydroxyethyl)-5-(3,4,5-trifluorophenyl)morpholine-4-carboxylic acid benzyl esterHCID 67373415—

반응 단계

Saturated sodium bicarbonate aqueous solution (20 mL) and benzyl chloroformate (1.31 mL) were added to a tetrahydrofuran (20 mL) solution of (R)-1-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]ethanol (2 g). After stirring the reaction solution for 16 hours at room temperature, additional benzyl chloroformate (1.33 mL) was added, and the resultant was further stirred for 20 hours. Water and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was removed under a vacuum. The residue was purified by silica gel column chromatography (heptane/ethyl acetate), and the title compound (880 mg) was obtained. The physical property values are as follows.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008293B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-c0d90e89cdf742cb928f5520b1f6b064
출처 메모uspto-grants-2011_08