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Aminoethylpiperazine → Benzyl (4,4-diethoxybutyl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Aminoethylpiperazine | HCID 8795 | — |
| 反応物 | Benzyl chloroformate | HCID 10387 | — |
| 反応物 | 4,4-Diethoxybutylamine | HCID 80672 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Sodium Carbonate | HCID 10340 | — |
| 生成物 | Benzyl (4,4-diethoxybutyl)carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06215002B1 |
| 出典データセット | uspto-grants-2001_04 |
| ORD ID | ord-914911e2d1354ed79d63067d7130b66e |
| 出典メモ | uspto-grants-2001_04 |