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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209614Generated: November 2, 2026

Ethanol → Ethyl 4-(bromomethyl)benzoate

https://huagongshe.com/reaction/2209614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-(Bromomethyl)benzoic acidHCID 22599—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(bromomethyl)benzoateHCID 954261—

Reaction Steps

To a stirred solution of 16.09 g (78 mmol) of 1,3-dicyclohexylcarbodiimide (Aldrich) in 100 ml methylene chloride was added a suspension of 15.4 g (71 mmol) of 4-carboxybenzylbromide in 100 ml methylene chloride and then 4.9 g (106.5 mmol) of absolute ethanol and 0.81 g (7.1 mmol) of 4-dimethylaminopyridine. A further 50 ml of methylene chloride was added to the reaction mixture and mixture heated at reflux for 2 hours. The mixture was allowed to cool to room temperature and the resultant white precipitate removed by filtration. The filtrate was washed with water, dried (MgSO4) and then concentrated in-vacuo to give the title compound as a colorless oil which crystallized on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455265
Source datasetuspto-grants-1995_10
ORD IDord-a9e63b87b2024216aede12dba4432bc6
Source noteuspto-grants-1995_10