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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974110Generated: October 29, 2026

Citric Acid → 2-(3,4-Dimethoxy-alpha-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethyl acetal

https://huagongshe.com/reaction/974110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantVeratraldehydeHCID 8419—
Reactant3,4,5-Trimethoxybenzaldehyde dimethyl acetalHCID 4193578—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product2-(3,4-Dimethoxy-alpha-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethyl acetalHCID 1059757396.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

136 ml of a 1.6M n-butyl lithium solution in hexane are added to a solution of 48.5 g of 3,4,5-trimethoxybenzaldehyde dimethyl acetal in 485 ml of benzene under stirring at 0° C. for about 20 minutes. The mixture is further stirred at 0° C. for 30 minutes, and 33.2 g of 3,4-dimethoxybenzaldehyde are added thereto. After stirring the mixture at 0° to 10° C. for 2 hours, 485 ml of water and 16 g of citric acid are added thereto. After shaking the mixture, the organic layer is separated therefrom, washed with water and evaporated under reduced pressure to remove solvent. 78.5 g of 2-(3,4-dimethoxy-α-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethyl acetal are thereby obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066825
Source datasetuspto-grants-1991_11
ORD IDord-9b7874ee5c484ebca0a87ed089300ef4
Source noteuspto-grants-1991_11