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HRID 233116作成日:2026年10月25日

Diethyl methylphosphonite → (4S)-3-benzyloxycarbonyl-4-{2-[ethoxy(methyl)phosphinyl]ethyl}-1,3-oxazolidin-5-one

https://huagongshe.com/reaction/233116

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl methylphosphoniteHCID 85063—
反応物(4S)-3-benzyloxycarbonyl-4-(2-bromoethyl)-1,3-oxazolidin-5-oneHCID 14103855—
生成物(4S)-3-benzyloxycarbonyl-4-{2-[ethoxy(methyl)phosphinyl]ethyl}-1,3-oxazolidin-5-oneHCID 1459628681.1%

反応条件

温度120 °C

反応手順

5.30 g (16.1 mmol) of (4S)-3-benzyloxycarbonyl-4-(2-bromomethyl)-1,3-oxazolidin-5-one (from Example 5) are mixed with 4.40 g (32.3 mmol) of diethyl methanephosphonite and the mixture is heated under argon for 6 hours at 120° C. The excess diethyl methanephosphonite is distilled off in high vacuum and the residue is purified by chromatography on silica gel (mobile phase: dichloromethane/acetonitrile). 4.64 g (81.1% of theory) of (4S)-3-benzyloxycarbonyl-4-{2-[ethoxy(methyl)phosphinyl]ethyl}-1,3-oxazolidin-5-one are obtained as a colorless oil. Analytical data:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591861
出典データセットuspto-grants-1997_01
ORD IDord-477b041f09a44fa0b19b83abb4644b6d
出典メモuspto-grants-1997_01