HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminoethylpiperazine → Benzyl (4,4-diethoxybutyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminoethylpiperazine | HCID 8795 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4,4-Diethoxybutylamine | HCID 80672 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | Benzyl (4,4-diethoxybutyl)carbamate | HCID 11471964 | — |
Reaction Steps
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 (1.6kg). T.l.c. (Ether) Rf 0.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057457 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-23d48274d99c4988a8c8e0e8038caf81 |
| Source note | uspto-grants-2000_05 |