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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458476Generated: November 2, 2026

Trimethyl orthoformate → 1-Bromo-4-(dimethoxymethyl)benzene

https://huagongshe.com/reaction/1458476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactant4-BromobenzaldehydeHCID 70741—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product1-Bromo-4-(dimethoxymethyl)benzeneHCID 688342—

Reaction Steps

21.1 g (114 mmol) of 4-bromobenzaldehyde and 20 ml (182 mmol) of trimethyl orthoformate (both Fluka, Buchs, Switzerland) are dissolved in 35 ml of methanol, and 0.65 g (3.4 mmol) of p-toluenesulfonic acid monohydrate is added at room temperature (exothermic reaction). The reaction mixture is stirred at room temperature under nitrogen for 20 hours. The acid is then neutralised with 0.62 ml of 30% sodium methanolate solution in methanol (3.4 mmol); the reaction mixture is concentrated using a rotary evaporator and the residue is distilled. The title compound is obtained in the form of a colourless liquid. TLC: Rt =0.58 (hexane/ethyl acetate 2:1). B.p.: 90°-92° C. (4 mbar). 1H-NMR (CDCl3 ; 200 MHz): 7.50 and 7.32/each d, J=9 (2×2H); 5.36/s (1H); 3.31/s (6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849911
Source datasetuspto-grants-1998_12
ORD IDord-e93d687c539945c58ecce39eabd6c4a6
Source noteuspto-grants-1998_12