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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354965Generated: October 31, 2026

Water → [2-(3-Methoxy-propoxy)-4-methyl-phenyl]-methanol

https://huagongshe.com/reaction/2354965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(3-Methoxypropoxy)-4-methylbenzaldehydeHCID 86053432—
SolventMethanolHCID 887—
Product[2-(3-Methoxy-propoxy)-4-methyl-phenyl]-methanolHCID 67542816—

Reaction Steps

To a solution of the title B compound, 2-(3-methoxy-propoxy)-4-methyl-benzaldehyde (3.7 g, 17.41 mmol) in 30 mL of methanol is added portion wise sodium borohydride (1.03 g, 26.12 mmol). The reaction mixture is stirred for 30 min at room temperature. Sodium borohydride (1.03 g, 26.12 mmol) is added and the mixture further stirred overnight to complete the reaction. After addition of H2O, the aqueous layer is extracted twice with ethyl acetate. The combined organic extracts are dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by flash column chromatography on silica gel (hexane/EtOAc 4/1 to 1/2) to afford the title compound as a colorless oil: TLC, Rf (hexane/AcOEt 2/1)=0.2. Rt (HPLC, Nucleosil C18, 10:90-100:0 CH3CN/H2O+0.1% TFA within 5 min, then 100% CH3CN+0.1% TFA): 4.88 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754727B2
Source datasetuspto-grants-2010_07
ORD IDord-24797b503bae4fc8a9dae0fbe262852d
Source noteuspto-grants-2010_07