HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Benzyl N-(4-hydroxybutyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-Amino-1-butanol | HCID 25868 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl N-(4-hydroxybutyl)carbamate | HCID 3366758 | 27.4% |
Reaction Steps
A solution of 4-amino-1-butanol (7.68 g) and pyridine (7.00 g) in dichloromethane (100 mL) was chilled in an ice bath and a solution of benzylchloroformate (14.37 g) in dichloromethane (100 mL) was slowly added with stirring over a period of thirty minutes. The ice bath was removed and the reaction was stirred for an additional 16 hours. Hydrochloric acid (1.2 M, 200 mL) was added and phases were separated. The organic phase was dried (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was recrystallized from toluene and dried under vacuum to provide 5.15 g of benzyl (4-hydroxybutyl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09107958B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9eb057dddaf64ecaaa387cad8408942b |
| Source note | uspto-grants-2015_08 |