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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821349Generated: October 29, 2026

(2-Methylsulfanylphenyl)methanol → 2-(Methylthio)benzaldehyde

https://huagongshe.com/reaction/1821349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methylsulfanylphenyl)methanolHCID 3551404—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product2-(Methylthio)benzaldehydeHCID 28644370.8%

Reaction Steps

To a solution of (2-methylsulfanylphenyl)methanol (0.20 g, 1.3 mmol) obtained in Step 1 in dichloromethane (4.0 mL), Celite (0.40 g) and pyridinium chlorochromate (0.42 g, 1.9 mmol) were added, followed by stirring at room temperature for 1.0 hour. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=95/5 to 80/20) to obtain 2-methylsulfanylbenzaldehyde (0.14 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605272B2
Source datasetuspto-grants-2009_10
ORD IDord-865e7276031540db982582d971c674f7
Source noteuspto-grants-2009_10