Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976629Generated: October 26, 2026

1-Bromopentane → 1-Benzyloxy-3-(4-butylphenyl)-1-pentylurea

https://huagongshe.com/reaction/976629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzyloxy-3-(4-butylphenyl)ureaHCID 19967368—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Benzyloxy-3-(4-butylphenyl)-1-pentylureaHCID 1996744562%

Reaction Steps

Sodium hydride (0.14 g of 80% in mineral oil, 4.7 mmol) was added to a solution of 1-benzyloxy-3-(4-butylphenyl)urea (1.25 g, 4.2 mmol) in N,N-dimethylformamide (5 mL). The reaction mixture was heated briefly on a steam bath under a nitrogen atmosphere. The reaction mixture was allowed to cool to ambient temperature then 1-bromopentane (0.63 g, 4.2 mmol) was added. The reaction mixture was heated at 90° C. overnight. The reaction mixture was cooled to ambient temperature, diluted with water and then extracted with diethyl ether. The organic layer was washed with water, dried with magnesium sulfate and then concentrated to provide 1.47 g of crude product as a brown oil. This material was purified by flash chromatography (silica gel; 1:19 ethyl acetate:hexanes) to provide 0.96 g of 1-benzyloxy-3-(4-butylphenyl)-1-pentylurea as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612377
Source datasetuspto-grants-1997_03
ORD IDord-161e249b100a4b4390ab9e5b292ca3c8
Source noteuspto-grants-1997_03