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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730167Generated: October 29, 2026

Methanol → (3-Methoxy-2-methylphenyl)methanol

https://huagongshe.com/reaction/730167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium borohydrideHCID 4148881—
Reactant3-Methoxy-2-MethylBenzoic AcidHCID 7021483—
SolventTetrahydrofuranHCID 8028—
Product(3-Methoxy-2-methylphenyl)methanolHCID 1557870999%

Reaction Steps

To a stirred mixture of LiBH4 (2.62 g; 120 mmol) in tetrahydrofuran (60 mL) was slowly added, via syringe, chlorotrimethylsilane (30.1 mL; 241 mmol). After stirring for 10 minutes, 3-methoxy-2-methylbenzoic acid (10.0 g, 60 mmol) was added in small portions. The mixture was stirred at ambient temperature for 18 hours. The mixture was cooled in an ice bath and methanol was slowly added until bubbling ceased and the solution turned clear. The reaction solution was evaporated to dryness. The residue was dispersed in dichloromethane and water. The phases were separated. The aqueous phase was basified with NaOH solution to pH 9-10 extracted with dichloromethane. The extracts were combined, dried over MgSO4, and evaporated to give (3-methoxy-2-methylphenyl)methanol 25, 9.10 g, 99% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582667B2
Source datasetuspto-grants-2009_09
ORD IDord-aa60eb022a804cffb0eea476434e0cbf
Source noteuspto-grants-2009_09