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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25299Generated: October 29, 2026

2-Methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrile → 2-Mercapto-4-(4-trifluoromethylphenyl)benzonitrile

https://huagongshe.com/reaction/25299

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrileHCID 22170951—
SolventTrifluoroacetic anhydrideHCID 9845—
Product2-Mercapto-4-(4-trifluoromethylphenyl)benzonitrileHCID 1213763751%

Reaction Steps

2.2 g (7.1 mmol) of 2-methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrile prepared in (b) was stirred in 15 ml of trifluoroacetic anhydride at room temperature for 12 hours, and the low-boiling matters were distilled off under reduced pressure. 50 ml of methanol and 3 g of 20% aqueous potassium hydroxide were added to the residue, and the reaction was carried out for 1 hour. The solvent was distilled off under reduced pressure, and the residue was mixed with 5% aqueous sulfuric acid and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 1.0 g of 2-mercapto-4-(4-trifluoromethylphenyl)benzonitrile (yield 51.0%), which was used in Example 1 as the starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-34368fc06629473d81e732cee37088b2
Source noteuspto-grants-2005_02