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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732940Generated: October 29, 2026

Hydrochloric Acid → 4-Methoxy-2-(propan-2-yl)phenol

https://huagongshe.com/reaction/732940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1-(2-Hydroxy-5-methoxyphenyl)ethan-1-oneHCID 69714—
ReactantHCID 178418332HCID 178418332—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-2-(propan-2-yl)phenolHCID 18364997—

Reaction Steps

To a cooled solution of 1-(2-Hydroxy-5-methoxy-phenyl)-ethanone (10.0 g) in 80 mL of THF was gradually added 46.4 g of 3M solution of MeMgCl in THF at a rate such that the reaction mixture temperature did not exceed 25 degrees C. Following addition of the MeMgCl solution, the reaction mixture was stirred at ambient temperature for 18 hours. To the stirred solution was then added 10% palladium on carbon (1.02 g, 50% water wet) suspended in 4 mL of THF. The reaction mixture was placed under a hydrogen atmosphere at 5 psig and cooling was applied to maintain a temperature of approximately 25° C. To the cooled mixture was gradually added concentrated HCl (20 mL) while maintaining the reaction temperature at 25° C. The resultant mixture was stirred at ambient temperature for 18 hours, then treated with 45 mL water and filtered through a bed of Celite to remove suspended catalyst. The filter cake was rinsed with EtOAc and the combined filtrate was separated. The organic phase was washed with water, then concentrated under reduced pressure to give 10.4 g of 2-isopropyl-4-methoxy-phenol, MS (M+H)=167. This product was dissolved in 2-butanone (20.4 g) and the crude solution was employed directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589090B2
Source datasetuspto-grants-2009_09
ORD IDord-8e83fef7a7c444e2baf63a4510daa9aa
Source noteuspto-grants-2009_09