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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3777생성일: 2026년 10월 24일

Boron trifluoride etherate → N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl ester

https://huagongshe.com/ko/reaction/3777

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물DiazomethaneHCID 9550—
반응물N-p-methoxybenzyloxycarbonyl-D-serine benzyl esterHCID 13652495—
반응물Acetone cardiceHCID 18522661—
용매DichloromethaneHCID 6344—
생성물N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl esterHCID 1365249770%

반응 단계

The N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester (720 mg, 2.00 mmol) is dissolved in dry dichloromethane (20 ml) and the solution cooled to dry ice/acetone. Boron trifluoride etherate (100 μl) is added followed by the portionwise addition of diazomethane (30 mmol in 20 ml CH2Cl2). After about 30 minutes the solution is filtered and washed once with water (10 ml), then dried (MgSO4) and evaporated to dryness. The resulting residue is chromatographed on silica gel using chloroform as eluant to give the pure title compound as an oil (520 mg, 70%) which crystallises on standing to give a colourless solid of m.p. 68°-69° C.; [α]D20 -1.3° (c 4.0, CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04722924
출처 데이터셋uspto-grants-1988_02
ORD IDord-3d9fe4eea0d14c78998610d953418f18
출처 메모uspto-grants-1988_02