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HRID 982494作成日:2026年10月26日

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

https://huagongshe.com/reaction/982494

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物DiazomethaneHCID 9550—
反応物N-p-methoxybenzyloxycarbonyl-D-serine benzyl esterHCID 13652495—
溶媒DichloromethaneHCID 6344—
溶媒Acetone cardiceHCID 18522661—
生成物N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl esterHCID 1365249770%

反応手順

The N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester (720 mg, 2.00 mmol) is dissolved in dry dichloromethane (20 ml) and the solution cooled in 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04996313
出典データセットuspto-grants-1991_02
ORD IDord-7d05f0a890b44fe78c85110c14523f5e
出典メモuspto-grants-1991_02