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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535681Generated: October 26, 2026

Bromine → 3-Bromo-2-hydroxy-5-methoxybenzaldehyde

https://huagongshe.com/reaction/535681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
Reactant2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product3-Bromo-2-hydroxy-5-methoxybenzaldehydeHCID 73581860%

Reaction Steps

To 2-hydroxy-5-methoxybenzaldehyde (4.1 mL, 32.86 mmol) in acetic acid (150 mL) were added sodium acetate (4.0 g, 49.3 mmol) and bromine (2.2 mL, 42.7 mmol) and the mixture was stirred at rt for 2 h. Aqueous sodium thiosulfate was added and the mixture was concentrated by rotary evaporation. The solid was dissolved in dichloromethane and washed with water. The organic phase was separated, dried over MgSO4, filtered and the solvent removed by rotary evaporation. The solid residue was recrystallized from ethanol to yield 3-bromo-2-hydroxy-5-methoxybenzaldehyde (4.55 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-8c00af4ab9564cd780c098b2589daae7
Source noteuspto-grants-2014_10