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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351819Generated: November 2, 2026

2,3,4-Trimethoxybenzaldehyde → (2,3,4-Trimethoxyphenyl)methanol

https://huagongshe.com/reaction/2351819

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-TrimethoxybenzaldehydeHCID 75006—
ReactantSodium borohydrideHCID 4311764—
ReactantCyclohexane ethylacetateHCID 21867204—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product(2,3,4-Trimethoxyphenyl)methanolHCID 123571—

Reaction Steps

2 g of commercials 2,3,4-trimethoxybenzaldehyde are placed in a 100 ml three-necked flask equipped with a magnetic stirrer, a gas inlet and a thermometer and are dissolved in 15 ml of CH2Cl2 +5 ml of ethanol. 200 mg of NaBH4 (6 mmoles) are added in small portions, at ambient temperature. The contents are stirred for 30 minutes at ambient temperature. TLC (cyclohexane:AcOEt 6:4) indicates a single-spot product. The ethanol is evaporated off and the residue is taken up with ChCl3, the organic phases are washed with NaCl and then with H2O, dried over MgSO4 and evaporated. An analytically pure pale yellow oil is obtained (Y=98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873349
Source datasetuspto-grants-1989_10
ORD IDord-d05e0023c8994e0f90127cd855485c48
Source noteuspto-grants-1989_10