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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594203Generated: November 3, 2026

Pyridine → Benzyl N-(4-hydroxybutyl)carbamate

https://huagongshe.com/reaction/594203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-Amino-1-butanolHCID 25868—
SolventDichloromethaneHCID 6344—
ProductBenzyl N-(4-hydroxybutyl)carbamateHCID 336675827.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242980B2
Source datasetuspto-grants-2016_01
ORD IDord-c01013e370bb4996929b4e3295b094de
Source noteuspto-grants-2016_01