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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501714Generated: October 25, 2026

Trimethyl orthoformate → 1-Bromo-2-(dimethoxymethyl)-4-methylbenzene

https://huagongshe.com/reaction/501714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Bromo-5-methylbenzaldehydeHCID 11845896—
SolventMethanolHCID 887—
Product1-Bromo-2-(dimethoxymethyl)-4-methylbenzeneHCID 6670499499%

Reaction Steps

Step AI (3): 2-Bromo-5-methylbenzaldehyde (500 mg, 2.51 mmol) was dissolved in methanol (5.0 mL). p-Toluenesulfonic acid monohydrate (90 mg, 0.52 mmol) and trimethoxymethane (5 mL) were added. The reaction mixture was heated at reflux for 5 h. The reaction mixture was extracted with DCM and washed with saturated aqueous sodium bicarbonate. The combined organic phases were dried over Na2SO4, filtered and concentrated in vacuum to yield 1-bromo-2-(dimethoxymethyl)-4-methylbenzene (615 mg, 99%) as a colorless oil. LC-MS (M−OCH3)+=213.25. 1H NMR (CD3OD, 500 MHz) δ 7.41-7.39 (m, 2H) 6.98 (d, J=10 Hz, 1H) 5.51 (s, 1H) 3.37 (s, 6H) 2.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772221B2
Source datasetuspto-grants-2010_08
ORD IDord-12f13d8064ba4300a6cd10f9a520d680
Source noteuspto-grants-2010_08