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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrile | HCID 22170951 | — |
| Solvent | Trifluoroacetic anhydride | HCID 9845 | — |
| Product | 2-Mercapto-4-(4-trifluoromethylphenyl)benzonitrile | HCID 12137637 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858639B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-34368fc06629473d81e732cee37088b2 |
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| Source note | uspto-grants-2005_02 |
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