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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453073Generated: October 30, 2026

(3-Methanesulfonylphenyl)methanol → 3-(Methylsulfonyl)benzaldehyde

https://huagongshe.com/reaction/1453073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Methanesulfonylphenyl)methanolHCID 23549738—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product3-(Methylsulfonyl)benzaldehydeHCID 1359660274.2%

Reaction Steps

A solution of [3-(methylsulfonyl)phenyl]methanol (680 mg, 3.66 mmol) in anhydrous CH2Cl2 (20 mL) was treated with PCC (1.03 g, 4.75 mmol) at room temperature for 2 hours. The solvent was removed and the residue was purified by flash column chromatography (20-60% EtOAc in hexanes) to give the product (500 mg, 74% yield). 1H NMR (300 MHz, CDCl3) δ: 3.13 (s, 3H), 7.77-7.82 (m, 1H), 8.18-8.24 (m, 2H), 8.46-8.48 (m, 1H), 10.12 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-ca06c370dc2942c1a5f0cfb0b8e0a2d2
Source noteuspto-grants-2009_01