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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170255Generated: October 25, 2026

Dicyclohexylcarbodiimide → Methyl 4-(bromomethyl)-3-nitrobenzoate

https://huagongshe.com/reaction/1170255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-Bromomethyl-3-nitrobenzoic acidHCID 132386—
Reactant4-pyridinemethanamine, N,N-dimethyl-HCID 264946—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
ProductMethyl 4-(bromomethyl)-3-nitrobenzoateHCID 13399987—

Reaction Steps

A solution of dicyclohexylcarbodiimide (DCC, 0.95 g, 4.61 mmol, 1.2 equiv) in 10 mL of dichloromethane (DCM) was added dropwise to a stirred mixture of 4-bromomethyl-3-nitro-benzoic acid 1 (1.0 g, 3.84 mmol, 1.0 equiv) and 4-dimethylaminomethylpyridine (DMAP) (0.020 g, 0.19 mmol, 0.05 equiv) in 10 mL of dichloromethane-methanol (10%) at room temperature. The mixture was stirred for 6 hours to obtain 4-bromomethyl-3-nitro-benzoic acid methyl ester 2. Dicyclohexyl urea (DCU) thus obtained was removed by filtration and the solvent in the filtered solution was removed under vacuum. The residue was purified by column chromatography using hexane-ethyl acetate (15%) as an eluant to give ester 2 as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825261B2
Source datasetuspto-grants-2010_11
ORD IDord-b2ed8b5eb7294125b0663e5aa2c912fc
Source noteuspto-grants-2010_11