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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037276Generated: October 27, 2026

Hydrochloric Acid → 3-Bromo-2-methoxybenzaldehyde

https://huagongshe.com/reaction/1037276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-2-hydroxybenzaldehydeHCID 10910555—
SolventDimethylformamideHCID 6228—
Product3-Bromo-2-methoxybenzaldehydeHCID 1106380894%

Reaction Steps

To a solution of 3-bromo-2-hydroxy-benzaldehyde (2.72 g, 13.53 mmol) in DMF (70 mL) were added potassium carbonate (5.61 g, 40.59 mmol) and iodomethane (1.01 mL, 16.24 mmol). The reaction mixture was stirred at RT. After 18 h, the mixture was acidified with cooling using 1 M HCl (aq), extracted with EtOAc. The organic extract was dried (Na2SO4), filtered and concentrated in vacuo to afford the title compound as an oil (2.73 g, 94%). 1H NMR (300 MHz, CDCl3): δ 10.36 (s, 1H), 7.85-7.79 (m, 2H), 7.15 (dt, J=7.7 and 0.7 Hz, 1H), 4.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-93087c2dc3e34bf09c9408daf7a60448
Source noteuspto-grants-2013_10