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HRID 585008作成日:2026年10月25日

Sodium Chloride → 3-(2-Ethoxyethanoyl)-4-benzyloxazolidin-2-one

https://huagongshe.com/reaction/585008

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Ethoxyacetyl chlorideHCID 84189—
反応物(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Ethoxyethanoyl)-4-benzyloxazolidin-2-oneHCID 21920117—

反応条件

温度-78 °C

反応手順

36.7 g (207 mmol) of (S)-4-benzyloxazolidin-2-one in 800 ml of THF are introduced into a round-bottomed flask under a stream of nitrogen. The reaction medium is cooled to −78° C. and 83 ml (207 mmol) of 2.5M n-butyllithium hexane are added dropwise. 30 minutes later, 25.4 g (207 mmol) of ethoxyacetyl chloride obtained in Example 81(b) are added, at −78° C. The reaction medium is stirred for 24 hours and then poured into saturated aqueous sodium chloride solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated. After purification by chromatography on a column of silica eluted with a heptane/ethyl acetate mixture (6/4), 30.6 g (56%) of the expected product are obtained in the form of an orange-colored oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06927228B2
出典データセットuspto-grants-2005_08
ORD IDord-87b9334d6a78453ab58a80b7a1cff62e
出典メモuspto-grants-2005_08