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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416179Generated: November 4, 2026

Methyl Benzoate → Trimethyl orthoformate

https://huagongshe.com/reaction/2416179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl BenzoateHCID 7150—
ReactantTributylmethylammoniumHCID 36209—
ReactantTetramethyl orthocarbonateHCID 74613—
SolventMethanolHCID 887—
ProductTrimethyl orthoformateHCID 9005—
ProductBenzaldehyde dimethyl acetalHCID 62375—

Reaction Steps

1062 g of tetramethoxymethane, 303 g of methyl benzoate, 225 g of 60% methyltributylammonium methosulfate solution and 910 g of methanol were electrolyzed at 3 A. The voltage per gap was kept below 5 V, the temperature was 30° C., and the pumping rate was 190 l/h. After the electrolysis had ended, 10.0 GC area % of trimethoxymethane and 13.2 GC area % of benzaldehyde dimethyl acetal had formed in the electrolyte; tetramethoxyethane had been degraded from 42.5% to 25.6 GC area %, and methyl benzoate was down to 0.4 GC area %, having been converted to more than 95%. Low-boiling byproducts included methyl formate at 2.2 GC area % in the electrolyte.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822124B2
Source datasetuspto-grants-2004_11
ORD IDord-ad31c5d3274e413788fc678a432849b9
Source noteuspto-grants-2004_11