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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390585Generated: October 25, 2026

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

https://huagongshe.com/reaction/390585

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-dimethylaminomethyl pyridine (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 numberUS08383662B2
Source datasetuspto-grants-2013_02
ORD IDord-ed0281c5bc0e43838b727eaf5f033ed9
Source noteuspto-grants-2013_02