HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminoethyl)pyrrolidine → tert-butyl N-[1-(pyrrolidin-3-yl)ethyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminoethyl)pyrrolidine | HCID 15228050 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl N-[1-(pyrrolidin-3-yl)ethyl]carbamate | HCID 14099015 | 99.1% |
Reaction Steps
640 mg of 1-benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminoethyl)pyrrolidine isomer (P-2A) and 300 mg of 5% Pd-C (50% wet) were added to 20 ml of ethanol and catalytic reduction was carried out at room temperature under 3 atm. for 3 h. Then, the catalyst was filtered off and ethanol was distilled off to obtain 390 mg of the desired compound (P-3A) in the form of a colorless, viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05098912 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-7ed34303c8d34cd69dd4f36f26ccb88e |
| Source note | uspto-grants-1992_03 |