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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357703Generated: November 3, 2026

Water → 3,4,5-Trimethoxybenzyl alcohol

https://huagongshe.com/reaction/357703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product3,4,5-Trimethoxybenzyl alcoholHCID 77449100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 500 ml round-bottom flask under nitrogen were added 15.32 g (0.41 mol) of sodium borohydride and 100 ml of dry tetrahydrofuran. The mixture was stirred for 10 min., then 20 g (0.108 mol) of 3,4,5-trimethoxybenzaldehyde dissolved in 100 ml of tetrahydrofuran was added dropwise to the solution described above. After stirring at room temperature for 16 hr, the solution was cooled to 0° C., 5 ml of distilled water was added dropwise, and the ice-bath was removed. The mixture was stirred overnight. Tetrahydrofuran was concentrated. The mixture was then diluted with 200 ml of water, and extracted twice with 200 ml of diethyl ether. The extract was dried over magnesium sulfate, concentrated after filtration, and dried in vacuum overnight. 3,4,5-Trimethoxybenzyl alcohol (20.2 g, 100% yield) was obtained as a colorless oil, which can be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840991
Source datasetuspto-grants-1998_11
ORD IDord-94db7a3636b04d208cb26797046ef25f
Source noteuspto-grants-1998_11