戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2190333作成日:2026年10月26日

Potassium Carbonate → Tert-butyl 4-(2-(3,3-diphenylpropylamino)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2190333

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1,1'-(3-Bromopropylidene)bisbenzeneHCID 88333—
反応物tert-Butyl 4-(2-aminoethyl)piperidine-1-carboxylateHCID 1514258—
溶媒AcetonitrileHCID 6342—
生成物Tert-butyl 4-(2-(3,3-diphenylpropylamino)ethyl)piperidine-1-carboxylateHCID 57586396—

反応条件

温度65 °C

反応手順

3-bromo-1,1-diphenylpropane (2.6 g, 9 mmol) and tert-butyl 4-(2-aminoethyl)piperidine-1-carboxylate (4.7 g, 21 mmol) were mixed together in acetonitrile (100 ml) and potassium carbonate (1.3 g, 9 mmol) was added. The resulting mixture was heated to 65° C. with stirring under N2 overnight. After that time the mixture was cooled and concentrated under reduced pressure. The residue was partitioned between DCM and water. The DCM layer was washed with water, dried over MgSO4 and concentrated under reduced pressure to give the crude product as a clear oil. The crude product was purified by combiflash (0-10% MeOH/DCM) to give tert-butyl 4-(2-(3,3-diphenylpropylamino)ethyl)piperidine-1-carboxylate 48.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08324396B2
出典データセットuspto-grants-2012_12
ORD IDord-8e62e59c5f8a4d2ab5c8ec216c75c717
出典メモuspto-grants-2012_12