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HRID 569362作成日:2026年10月26日

Acetic acid, 2-chloro-, phenylmethyl ester → Tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate

https://huagongshe.com/reaction/569362

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid, 2-chloro-, phenylmethyl esterHCID 8786—
反応物Potassium CarbonateHCID 11430—
反応物tert-butyl 2-hydroxyimino-3-oxobutanoateHCID 178468384—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrateHCID 5381166595.3%

反応条件

温度40 °C

反応手順

To a suspension of tert-butyl 2-hydroxyimino-3-oxobutyrate (56.4 g) and potassium carbonate (62.4 g) in ethyl acetate (300 ml) and N,N-dimethylformamide (60 ml) was added benzyl chloroacetate (60 g), and the mixture was stirred at 40° C. for 7 hours. The reaction mixture was poured into ice-water (1000 ml), and the separated organic layer was washed twice with a saturated aqueous solution of sodium chloride and then dried over magnesium sulfate. Removal of the solvent gave tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate (96.3 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04731443
出典データセットuspto-grants-1988_03
ORD IDord-3228b8bd8b25419a9f5eca11a38f91e4
出典メモuspto-grants-1988_03