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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597884Generated: November 4, 2026

3-Hydroxybenzaldehyde → 3-(2-Bromoethoxy)benzaldehyde

https://huagongshe.com/reaction/1597884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantAcetonitrileHCID 6342—
Reactant1,1-DibromoethaneHCID 11201—
ReactantPotassium CarbonateHCID 11430—
SolventDiethyl EtherHCID 3283—
Product3-(2-Bromoethoxy)benzaldehydeHCID 2735565—

Reaction Steps

A mixture of 3-hydroxybenzaldehyde (5.17 g, 42.33 mmol), K2CO3 (58.5 g) and CH3CN (100 ml) was stirred at room temperature for 15 minutes, then dibromoethane (18.3 ml) was added. The reaction mixture was stirred at room temperature for 30 minutes, then at reflux for 3-4 hours. Additional dibromoethane was added and then the reaction mixture was refluxed overnight. The reaction mixture was cooled, filtered, and the filtrate was stripped to afford an oil. The oil was dissolved in ether (300 ml), washed with 5N NaOH (2×75 ml) and the ether layer was dried over MgSO4 and stripped. The residue was purified by column chromatography on silica gel eluting with 10% ethyl acetate/hexane to afford 5.23 g of 3-(2-bromoethoxy)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-85db9d3d72684d92985a166fe044ee69
Source noteuspto-grants-1998_04