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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974111Generated: October 31, 2026

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

https://huagongshe.com/reaction/974111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantVeratraldehydeHCID 8419—
Reactant3,4,5-Trimethoxybenzaldehyde dimethyl acetalHCID 4193578—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(3,4-Dimethoxy-alpha-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethyl acetalHCID 1059757397.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

136 ml of a 1.6M n-butyl lithium solution in toluene are added to a solution of 48.5 g of 3,4,5-trimethoxybenzaldehyde dimethyl acetal in 485 ml of tetrahydrofuran 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, 780 ml of water and 780 ml of ethyl acetate are added thereto. After shaking the mixture, the organic layer is separated therefrom, washed with water and evaporated under reduced pressure to remove solvent. 79.5 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-006c2c158d514df4be890a0b5949011c
Source noteuspto-grants-1991_11