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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393580Generated: October 25, 2026

Water → 3-Bromo-2,5-dimethoxybenzyl Alcohol

https://huagongshe.com/reaction/2393580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant3-Bromo-2,5-dimethoxybenzaldehydeHCID 931096—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Bromo-2,5-dimethoxybenzyl AlcoholHCID 10192777100%

Reaction Steps

A solution of 8.27 gm (33.75 mmol) of 3-bromo-2,5-dimethoxy benzaldehyde* in 40 ml THF and 20 ml water was cooled to 10° C. and treated portionwise with 3.83 gm (101.2 mmol) NaBH4. Stirring was maintained at ambient temperature until tlc analysis (silica gel; 1:4 ethyl acetate:hexane) indicated the absence of starting aldehyde. After 30 minutes the solvent was removed in vacuo and the residue was portioned between ethyl acetate and water. After washing with brine and drying (Na2SO4), the ethyl acetate extract was concentrated in vacuo to yield 8.34 gm (99%) of a white solid, mp 59°-60° C.; tlc (cited), Rf 0.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807897
Source datasetuspto-grants-1998_09
ORD IDord-6abe74e3c66a411596eb4c01c542510a
Source noteuspto-grants-1998_09