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HRID 37264作成日:2026年10月24日

Hydrochloric Acid → 2-(4-Nitrobenzyloxycarbonyl)amino-1,3-propanediol

https://huagongshe.com/ja/reaction/37264

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物methyl (2S)-3-hydroxy-2-[(4-nitrobenzyloxycarbonyl)amino]propionateHCID 57056522—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-(4-Nitrobenzyloxycarbonyl)amino-1,3-propanediolHCID 1993452268.7%

反応条件

温度0 °C

反応手順

To a solution of methyl (2S)-3-hydroxy-2-[(4-nitrobenzyloxycarbonyl)amino]propionate (2.12 g) in tetrahydrofuran (20 ml) and ethanol (20 ml) was added sodium borohydride (0.54 g) at 0° C. under nitrogen atmosphere. After stirring at 0° C. for 5 hours, to the mixture was added a mixture of concentrated hydrochloric acid (1.7 ml), water (40 ml) and ethyl acetate (40 ml). The organic layer was separated, washed with 10% aqueous sodium hydrogen carbonate and brine successively, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel (160 ml) eluting with a mixture of acetone and dichloromethane (1:9, V/V) to give 2-[(4-nitrobenzyloxycarbonyl)amino]-1,3-propanediol (1.32 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420122
出典データセットuspto-grants-1995_05
ORD IDord-f60d992394f548f6afb91dbb556f5626
出典メモuspto-grants-1995_05