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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602379Generated: October 26, 2026

Triethylamine → 1-Bromo-5-(dimethoxymethyl)-4-fluoro-2-methoxybenzene

https://huagongshe.com/reaction/602379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethyl orthoformateHCID 9005—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant5-Bromo-2-fluoro-4-methoxybenzaldehydeHCID 12187210—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product1-Bromo-5-(dimethoxymethyl)-4-fluoro-2-methoxybenzeneHCID 67061307100%

Reaction Steps

5-Bromo-2-fluoro-4-methoxybenzaldehyde (1 g, 4.3 mmol), p-toluenesulfonic acid monohydrate (163 mg, 0.86 mmol) and trimethyl orthoformate (2.4 mL, 21 mmol) were dissolved in methanol (20 mL) and stirred under heating and reflux for 1 hour. After standing to cool the reaction mixture, triethylamine (2 mL) was added thereto and further stirred for 10 minutes. The mixture was added with saturated brine and ethyl acetate, and the organic layer was separated, followed by washing with saturated brine. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to obtain 5-bromo-2-fluoro-4-methoxybenzaldehyde dimethylacetal (1.19 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906522B2
Source datasetuspto-grants-2011_03
ORD IDord-07cd30235450420b9174ade536a6948d
Source noteuspto-grants-2011_03