HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → 2-(1-Pyrrolidinyl)carbonyl-1-benzylpyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Benzyl-L-proline | HCID 728719 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Pyrrolidinyl)carbonyl-1-benzylpyrrolidine | HCID 23282646 | 53.9% |
Reaction Steps
A solution of 1-benzyl-L-proline (50 g) in dichloromethane (300 ml) is cooled with ice. To the solution is added N-methylmorpholine (22.5 g), and then further thereto is added dropwise isobutyl chloroformate (30 g). The mixture is stirred at the same temperature for about one hour, and thereto is added dropwise pyrrolidine (18.8 ml) at the same temperature. The mixture is warmed to room temperature, and stirred for two days. The mixture is washed twice with water (250 ml), and dried over magnesium sulfate. The mixture is concentrated under reduced pressure, and the residue is recrystallized from ethyl acetate-n-hexane to give 2-(1-pyrrolidinyl)carbonyl-1-benzylpyrrolidine (31 g), as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140330 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-520efe8c1c574273821a2b313e60c990 |
| Source note | uspto-grants-2000_10 |