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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501717Generated: October 25, 2026

Ethyl orthoformate → HCID 15114404, compound

https://huagongshe.com/reaction/501717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Bromo-5-(trifluoromethyl)benzaldehydeHCID 7018047—
SolventMethanolHCID 887—
ProductHCID 15114404HCID 1511440471%

Reaction Steps

Step AJ (1): 2-Bromo-5-(trifluoromethyl)benzaldehyde (1069 mg, 4.975 mmol) was dissolved in a mixture of methanol (20 mL) and triethylorthoformate (20 mL). p-Toluenesulfonic acid monohydrate (180.0 mg, 0.946 mmol) was added and the reaction mixture was stirred under reflux for 5 h. The reaction was quenched with aqueous NaHCO3 and extracted with DCM. The combined organic phases were dried over Na2SO4, filtered and concentrated in vacuum at the temperature, not exceeding 35° C. The residue was purified by silica gel chromatography to give 1-bromo-2-(dimethoxymethyl)-4-methoxybenzene (1060 mg, 71%) as a colorless oil. LC-MS (M−OCH3)+=267.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772221B2
Source datasetuspto-grants-2010_08
ORD IDord-25ca6c9a1559491c99e95eb8418e6fef
Source noteuspto-grants-2010_08