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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821557Generated: October 26, 2026

Dichloromethane → 4.5-Dimethoxy-2-nitrobenzyl 2-bromoacetate

https://huagongshe.com/reaction/1821557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactant6-Nitroveratryl alcoholHCID 66097—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
Product4.5-Dimethoxy-2-nitrobenzyl 2-bromoacetateHCID 8607121955.1%

Reaction Steps

Bromoacetylbromide (0.19 ml, 2.2 mmol) was slowly added to the solution of 6-nitroveratrylalcohol (0.43 g, 2 mmol), Et3N (0.56 ml, 4 mmol) and DMAP (24 mg, 0.2 mmol) in CHCl3 (5 ml). After stirring at room temperature for five hours, CH2Cl2 (20 ml) was added and the mixture was washed with HCl (1 M, 2×10 ml), NaHCO3 (sat., 10 ml) and water (10 ml). Organic phase was dried over Na2SO4, evaporated and purified by chromatography (Si-gel, CH2Cl2) to yield 4.5-dimethoxy-2-nitrobenzyl 2-bromoacetate (368 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608582B2
Source datasetuspto-grants-2009_10
ORD IDord-33a2afce51674e87b3b73355ac518a23
Source noteuspto-grants-2009_10