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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204203Generated: October 27, 2026

Benzyl Bromide → Benzyl 4-bromo-3-methoxybenzoate

https://huagongshe.com/reaction/2204203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3-methoxybenzoic acidHCID 16215867—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-bromo-3-methoxybenzoateHCID 5855148091%

Reaction Steps

4-Bromo-3-methoxy-benzoic acid (1.50 g, 6.49 mmol), K2CO3 (2.69 g, 19.5 mmol), and DMF (10 mL) were combined and the mixture was allowed to stir for 10 minutes. Bromomethylbenzene (849 μL, 7.14 mmol) was added dropwise and the mixture was allowed to stir at rt for 1 h. The reaction mixture was quenched with brine and was extracted with EtOAc (3×). The organic layers were dried over sodium sulfate, filter and concentrated. The residue was purified using silica gel chromatography (5%-70% EtOAc in hexanes) to provide benzyl 4-bromo-3-methoxybenzoate (91%). ESI-MS m/z calc 320.0, found 321.0/323.0 (M+1)+. Retention time: 3.24 minutes (4 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-72867144bd36423692350dac45f1f062
Source noteuspto-grants-2016_06