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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic acid, 2-chloro-, phenylmethyl ester | HCID 8786 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | tert-butyl 2-hydroxyimino-3-oxobutanoate | HCID 178468384 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate | HCID 53811665 | 95.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04731443 |
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| 出典データセット | uspto-grants-1988_03 |
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| ORD ID | ord-3228b8bd8b25419a9f5eca11a38f91e4 |
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| 出典メモ | uspto-grants-1988_03 |
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