HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25288Generated: October 30, 2026
Sodium Hydroxide → 2-Cyclopropylmethylthio-4-(5-trifluoromethylpyridin-2-yl)benzonitrile
https://huagongshe.com/reaction/25288
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [(Cyclopropylmethyl)sulfanyl]methanimidamide hydrobromide | HCID 2777025 | — |
| Reactant | HCID 22170891 | HCID 22170891 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Cyclopropylmethylthio-4-(5-trifluoromethylpyridin-2-yl)benzonitrile | HCID 22170894 | 96.8% |
Reaction Steps
1.8 g (6.8 mmol) of 4-(5-trifluoromethylpyridin-2-yl)-2-fluorobenzonitrile, 1.6 g (7.6 mmol) of S-cyclopropylmethylisothiourea hydrobromide salt and 50 ml of N,N-dimethylformamide were put into a round-bottomed flask and stirred together with 1.6 g (B mmol) of 20% aqueous sodium hydroxide overnight. The solvent was distilled off under reduced pressure, and the reaction mixture was separated with 50 ml of water and 50 ml of ethyl acetate. The organic layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 2.2 g of 2-cyclopropylmethylthio-4-(5-trifluoromethylpyridin-2-yl)benzonitrile (yield 96%) as pale yellow feathery crystals (m.p. 135-136° C.).
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-2287a12e884b462b847ca54a0969e0df |
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| Source note | uspto-grants-2005_02 |
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