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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357707Generated: October 26, 2026

Acetic Acid → 4-((3,4,5-Trimethoxybenzyl)sulfinyl)phenol

https://huagongshe.com/reaction/357707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-((3,4,5-Trimethoxybenzyl)thio)phenolHCID 384136—
Catalystchromium (VI) trioxideHCID 10219390—
SolventWaterHCID 962—
Product4-((3,4,5-Trimethoxybenzyl)sulfinyl)phenolHCID 38413766%

Reaction Conditions

Temperature80 °C

Reaction Steps

3,4,5-Trimethoxybenzyl 4-hydroxyphenyl thioether (500 mg, 1.63 mmol), prepared as described in Example 1, was dissolved in 10 mlof acetic acid, and heated to 80° C. A solution of chromium trioxide in 30 ml of distilled water was added dropwise to the above solution. The mixture was stirred for 30 min, cooled to room temperature, diluted with 20 ml of water, and then extracted with 30 ml of ethyl acetate. The organic layer was dried over magnesium sulfate, concentrated and purified on silica gel column chromatography (ethyl acetate/n-hexane=1/4) to give 348 mg (66% yield) of 3,4,5-trimethoxybenzyl 4-hydroxyphenyl sulfoxide as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840991
Source datasetuspto-grants-1998_11
ORD IDord-e92c83b6fc5c41b6952ad2903c7a142b
Source noteuspto-grants-1998_11