HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 3-Acetylaminomethyl-1-benzyl-4-chloropyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Aminomethyl-1-benzyl-4-chloropyrrolidine | HCID 13959895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Acetylaminomethyl-1-benzyl-4-chloropyrrolidine | HCID 13913008 | 78.3% |
Reaction Steps
To 3-aminomethyl-1-benzyl-4-chloropyrrolidine (2.69 g) is added ethanol (50 ml) and thereto is added dropwise acetyl chloride (1.02 g) with stirring under ice-cooling. The mixture is stirred at room temperature overnight, then concentrated, neutralized with saturated aqueous sodium hydrogen carbonate, and extructed with dichloromethane. The dichloromethane layer is dried and concentrated to give 3-acetylaminomethyl-1-benzyl-4-chloropyrrolidine (2.50 g) as an yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04786649 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-ada00a0e55684e659624752873a26ccc |
| Source note | uspto-grants-1988_11 |