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HRID 486436作成日:2026年10月26日

Ethyl chloroformate → Ethyl 3-methyl-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/486436

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl chloroformateHCID 10928—
反応物1-Benzyl-3-methyl-4-piperidoneHCID 560965—
溶媒TolueneHCID 1140—
生成物Ethyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 1507565783%

反応手順

To a stirred solution of 152 parts of 3-methyl-1-(phenylmethyl)-4-piperidinone in 900 parts of methylbenzene were added dropwise 218 parts of ethyl carbonochloridate at room temperature. Upon completion, stirring was continued overnight at reflux. After cooling, the reaction mixture was washed with water and hydrochloric acid, dried, filtered and evaporated. The residue was distilled, yielding 120.5 parts (83%) of ethyl 3-methyl-4-oxo-1-piperidinecarboxylate; bp. 98°-105° C. at 1 mm pressure (intermediate 26).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292738
出典データセットuspto-grants-1994_03
ORD IDord-abcf0f1d31534ab2b8f0fd36767139f3
出典メモuspto-grants-1994_03