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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405403Generated: October 27, 2026

Benzyl Bromide → Benzyl 4-bromo-3-methoxybenzoate

https://huagongshe.com/reaction/1405403

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 gL, 7.14 mmol) was added dropwise and the mixture was allowed to stir at room temperature 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+I)+. Retention time: 3.24 minutes (4 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916565B2
Source datasetuspto-grants-2014_12
ORD IDord-d613949bcf644ac7a92c4f1992213515
Source noteuspto-grants-2014_12