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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770608Generated: October 30, 2026

3-(Bromomethyl)benzaldehyde → 3-(Methoxymethyl)benzaldehyde

https://huagongshe.com/reaction/1770608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)benzaldehydeHCID 7127825—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
Product3-(Methoxymethyl)benzaldehydeHCID 1224562374%

Reaction Steps

3-(bromomethyl)benzaldehyde (1.00 g, 5.02 mmol) was dissolved in MeOH (100 mL) and treated with 0.5M solution of MeONa (5 equiv.) in MeOH. The mixture was stirred overnight at RT and MeOH was evaporated under reduced pressure. The residue was acidified to pH ˜6 with 1M aqueous HCl solution. DCM (100 mL) was added and the mixture was vigorously stirred overnight. The organic layer was separated, dried over Na2SO4 and the solvent was removed under reduce pressure to furnish the desired material as yellowish oil (560 mg, 3.75 mmol, 74%). 1H NMR (DMSO, 400 MHz): δ3.33 (s, 3H), 4.51 (s, 1H), 7.62 (m, 2H), 7.85 (m, 2H), 10.02 (s, 1H). MS 151 (MH1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09247759B2
Source datasetuspto-grants-2016_02
ORD IDord-5e10d825fd674490bc0167706867cf4e
Source noteuspto-grants-2016_02