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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324033Generated: October 26, 2026

Trimethyl orthoformate → 1-Bromo-2-(dimethoxymethyl)-4,5-dimethoxybenzene

https://huagongshe.com/reaction/324033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactant6-Bromo-3,4-dimethoxybenzaldehydeHCID 79351—
SolventMethanolHCID 887—
Product1-Bromo-2-(dimethoxymethyl)-4,5-dimethoxybenzeneHCID 11077146—

Reaction Steps

6-Bromo-3,4-dimethoxybenzaldehyde (470 g) is suspended in methanol (600 ml), and thereto are added trimethyl orthoformate (1025 ml) and IRA-120 (H+-type, 10 g), and the mixture is refluxed for one hour. The mixture is cooled to room temperature, and the insoluble materials are removed by filtration, and the filtrate is concentrated under reduced pressure. The resulting residue is dissolved in ether, washed, dried, evaporated to remove the ether, and distilled under reduced pressure to give 6-bromo-3,4-dimethoxybenzaldehyde dimethyl acetal (522 g) as a main distillate (133-138° C./1 Torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214996B1
Source datasetuspto-grants-2001_04
ORD IDord-311d3a0a51d0408b98f9608191981361
Source noteuspto-grants-2001_04