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HRID 712207作成日:2026年10月24日

Hexane → 1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate

https://huagongshe.com/ja/reaction/712207

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
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 5775037648%

反応条件

温度-78 °C

反応手順

A solution of tert-butyl 4-cyanopiperidine-1-carboxylate (0.75 g, 3.57 mmol) in THF (25.0 mL) was cooled to −78° C. followed by dropwise addition of LDA (1.8 M in THF, 6.0 mL, 5.35 mmol) and stirred at the same temperature (−78° C.) for 45 min followed by addition of ethyl chloroformate (0.46 g, 4.28 mmol). The temperature of the reaction was slowly raised to rt and left to stir for 6 h. The reaction was then cooled to 0° C. and quenched by drop wise addition of saturated NH4Cl solution (50 mL), extracted with EtOAc (3×100 mL) and the combined organics washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude residue was purified over 100-200 M silica-gel using 7% EtOAc:hexane to obtain the product as an orange viscous liquid (0.4 g, 48% yield). MS: 283.14 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181234B2
出典データセットuspto-grants-2015_11
ORD IDord-09798f3e46594c668a7a06e7d4b56e82
出典メモuspto-grants-2015_11