戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 3777作成日:2026年10月23日

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

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

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—
反応物Acetone cardiceHCID 18522661—
溶媒DichloromethaneHCID 6344—
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 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04722924
出典データセットuspto-grants-1988_02
ORD IDord-3d9fe4eea0d14c78998610d953418f18
出典メモuspto-grants-1988_02