Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599794Generated: October 31, 2026

Water → 3,4,5-Trimethoxybenzyl alcohol

https://huagongshe.com/reaction/599794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantSodium borohydrideHCID 4311764—
Product3,4,5-Trimethoxybenzyl alcoholHCID 7744992.72%

Reaction Conditions

Temperature40 °C

Reaction Steps

Adding 3,4,5-trimethoxybenzaldehyde (15 g, 76.45 mmol) and anhydrous alcohol (200 ml) in the three-necked bottle (250 ml), heating to 40° C. to dissolve, adding sodium borohydride (1.48 g, 38.23 mmol), heating to reflux for 45 minutes, and monitored by TLC. When the reaction is completed, cooling it to room temperature, adding deionized water (10 ml, 555.8 mol), to quench the reaction and suction filtering, washing the filter residue by anhydrous alcohol (20 ml), conflating the filtrate, concentrating in rotarory evaporater to dry, adding dichlormethane (100 ml) to dissolve, washing with sodium hydroxide solution (50 ml) twice and with deionized water (50 ml) twice, adding proper amount of anhydrous magnesium sulfate to dry overnight, filtering, washing the filter residue with dichlormethane (20 ml), conflating the filtrate, concentrating in rotarory evaporater to dry to get 3,4,5-trimethoxyl benzyl alcohol, 14.05 g of colorless oily product), the yield: 92.72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897820B2
Source datasetuspto-grants-2011_03
ORD IDord-5810dc733538412393ecb3dcb9ce10d7
Source noteuspto-grants-2011_03