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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974108Generated: November 1, 2026

3,4,5-Trimethoxybenzaldehyde → 3,4,5-Trimethoxybenzaldehyde dimethyl acetal

https://huagongshe.com/reaction/974108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium MethoxideHCID 10942334—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product3,4,5-Trimethoxybenzaldehyde dimethyl acetalHCID 4193578100.3%

Reaction Steps

A mixture of 196.2 g of 3,4,5-trimethoxybenzaldehyde, 127.3 g of trimethoxymethane, 200 ml of methanol and 0.1 g of hydrochloric acid is refluxed for 3 hours. After cooling the reaction mixture, 0.2 g of a 24% sodium methoxide solution in methanol is added thereto and the mixture is evaporated under reduced pressure to remove solvent. 150 ml of tetrahydrofuran are added to the residue, and the mixture is evaporated under reduced pressure to remove solvent. 243 g of 3,4,5-trimethoxybenzaldehyde dimethyl acetal are thereby obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066825
Source datasetuspto-grants-1991_11
ORD IDord-eac34bc471ee4134868a9133acfe0832
Source noteuspto-grants-1991_11