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HRID 1611148作成日:2026年10月25日

Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate → tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1611148

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylateHCID 69249758—
溶媒Formic AcidHCID 284—
生成物tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylateHCID 2225894760%

反応手順

tert-Butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate (1.16 g, 4.81 mmol) was dissolved in 90% formic acid (2 mL). The mixture was stirred at room temperature for 40 min. The mixture was then partitioned between ethyl acetate and saturated aqueous NaHCO3 solution. The separated organic phase was washed with brine, dried over Na2SO4, filtered and evaporated. Purification by column chromatography (hexane/ethyl acetate=4/1) gave tert-butyl 3-(2-oxoethyl)-1-piperidinecarboxylate as a colorless oil (652 mg, yield; 60%). [Starting Compound 2H]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06984649B1
出典データセットuspto-grants-2006_01
ORD IDord-dfa4cf42235448b9bb08d335f6b60f00
出典メモuspto-grants-2006_01