Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957956Generated: November 2, 2026

Sodium methanesulfinate → 1-Methylsulfonylmethyl-3-nitro-5-trifluoromethyl-benzene

https://huagongshe.com/reaction/1957956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanesulfinateHCID 2733271—
Reactant1-(Chloromethyl)-3-nitro-5-(trifluoromethyl)benzeneHCID 68425095—
SolventMethanolHCID 887—
Product1-Methylsulfonylmethyl-3-nitro-5-trifluoromethyl-benzeneHCID 6842330492.2%

Reaction Steps

A solution of 1-chloromethyl-3-nitro-5-trifluoromethyl-benzene (520 mg; 2.170 mmol) and methanesulfinic acid sodium salt (664 mg; 6.511 mmol) in Methanol (10 ml) of was refluxed overnight. The reaction was then cooled to room temperature and the product precipitated was filtered and diluted with dichloromethane. The solid was removed and the organic phase was concentrated in vacuo 520 mg (2 mmol; 85% yield) of 1-methylsulfonylmethyl-3-nitro-5-trifluoromethyl-benzene were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410100B2
Source datasetuspto-grants-2013_04
ORD IDord-c521c703272c4832b7d389f592e4fd42
Source noteuspto-grants-2013_04