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HRID 423027作成日:2026年10月27日

Ethyl chloroformate → 1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/423027

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Tert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylateHCID 5775037651.6%

反応条件

温度-78 °C

反応手順

A solution of LDA (107 ml, 214.01 mmol) was added to a stirred solution of tert-butyl 4-cyanopiperidine-1-carboxylate (30 g, 143 mmol) in THF (250 ml) at −78° C., under nitrogen. The resulting solution was stirred at −78° C. for 30 minutes. Ethyl chloroformate (16.37 ml, 171.2 mmol) was added. The resulting solution was stirred and allowed to warm to room temperature. The reaction mixture was quenched with saturated NaHCO3 (250 ml), extracted with DCM, and the organic layer was washed with saturated brine (100 ml) then dried over MgSO4, filtered and evaporated to afford the crude material as a orange oil. This material was purified by flash silica chromatography, elution gradient 10% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford 1-tert-butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate (20.8 g, 51.6%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101623B2
出典データセットuspto-grants-2012_01
ORD IDord-e521e8be4e0f43de9130e9c71b98b0b5
出典メモuspto-grants-2012_01