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HRID 323997作成日:2026年10月25日

Aminoethylpiperazine → Benzyl (4,4-diethoxybutyl)carbamate

https://huagongshe.com/reaction/323997

反応式

関与物質

役割名称HCID仕込み量
反応物AminoethylpiperazineHCID 8795—
反応物Benzyl chloroformateHCID 10387—
反応物4,4-DiethoxybutylamineHCID 80672—
溶媒DichloromethaneHCID 6344—
溶媒Sodium CarbonateHCID 10340—
生成物Benzyl (4,4-diethoxybutyl)carbamateHCID 11471964—

反応手順

Three portions of benzyl chloroformate (260 ml) in dichloromethane (170 ml) were added sequentially over 1 h 40 min to a vigorously stirred mixture of 4-aminobutyraldehyde diethyl acetal (910 ml) in dichloromethane (3 l ) and aqueous sodium carbonate (1M, 3 l). Stirring was continued for 50 min until gas evolution ceased. N-(2-aminoethyl)piperazine (40 ml) was added and stirring was continued for 1 h 15 min. The layers were separated and the organic layer was washed with aqueous citric acid (1M, 3.8 l) and saturated aqueous sodium bicarbonate (2 l), dried (MgSO4), filtered and concentrated in vacuo to give the title compound as a yellow oil (1.6 kg). T.l.c. (Ether) Rf 0.5.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06215002B1
出典データセットuspto-grants-2001_04
ORD IDord-914911e2d1354ed79d63067d7130b66e
出典メモuspto-grants-2001_04