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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376333Generated: October 26, 2026

Hydrochloric Acid → 2-Hydroxy-4'(methylthio)isobutyrophenone

https://huagongshe.com/reaction/376333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbon TetrachlorideHCID 5943—
ReactantSodium HydroxideHCID 14798—
Reactant2-Methyl-1-[4-(methylthio)phenyl]-1-propanoneHCID 852539—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product2-Hydroxy-4'(methylthio)isobutyrophenoneHCID 11413168—

Reaction Conditions

Temperature15 °C

Reaction Steps

To a solution of 2-methyl-1-(4-(methylthio)phenyl)propan-1-one (28.5 g, 147 mmol, Step 1), Aliquat 336 (11.0 mL, 24 mmol) and carbon tetrachloride (21 mL, 218 mmol) in toluene (43 mL) was added sodium hydroxide (12.9 g, pellets, 322 mmol). The reaction was stirred at 15° C. for 2 h and then at r.t. for 16 h. The reaction was diluted with water (100 mL), brine (100 mL) and EtOAc (300 mL). The aqueous phase was acidified with 1 N HCl and extracted with EtOAc (100 mL). The combined organic layers were dried over Na2SO4 and concentrated. The crude product was purified by silica gel chromatography eluted with 15% EtOAc in hexane to give the title compound as a thick syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020343
Source datasetuspto-grants-2000_02
ORD IDord-f7f1986c25c24634a617f4cb2e83a79e
Source noteuspto-grants-2000_02