HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566639Generated: October 28, 2026
Stannous chloride dihydrate → 2-[(Trifluoromethyl)thio]aniline
https://huagongshe.com/reaction/566639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 2-nitrophenyl trifluoromethyl sulfide | HCID 9815915 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(Trifluoromethyl)thio]aniline | HCID 67670 | 75.7% |
Reaction Steps
A solution of 25.53 g of tin(II) chloride dihydrate in 40 ml of concentrated hydrochloric acid was added dropwise to a stirred solution of 5.05 g of 2-nitrophenyl trifluoromethyl sulfide, obtained according to Example 1, in 30 ml of ethanol. After the addition had ended, the mixture was heated to 100° C. and stirred at this temperature for 1.5 hours. The mixture was cooled, ethanol was evaporated off under reduced pressure, and the residue was poured into a mixture of 150 g of ice and 150 ml of 40% strength by weight aqueous sodium hydroxide solution. The product was extracted with ether. The combined ether extracts were dried over magnesium sulfate and concentrated under reduced pressure. Vacuum distillation of the residue gave 3.31 g (75.7% of theory) of 2-aminophenyl trifluoromethyl sulfide (boiling point 102-104° C. at 50 mbar, melting point: 30-31° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06175042B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-3bf0986a95094df794209f16e30c6c5a |
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| Source note | uspto-grants-2001_01 |
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