HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989243Generated: October 29, 2026
2-Chloroethyl methyl sulfide → HCID 18005372, compound
https://huagongshe.com/reaction/989243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl methyl sulfide | HCID 10965 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | Ethiprole | HCID 9930667 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18005372 | HCID 18005372 | 4.4% |
Reaction Steps
To a suspension of 35% potassium hydride in oil (1.4 g) in dry N,N-dimethylformamide (DMF) was added a solution of 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-amino-4-(ethylsulfinyl)-1H-pyrazole-3-carbonitrile (5.0 g) in dry DMF at 4° C. and stirred for 40 min. 2-Chloroethyl methyl sulfide (1.39 g) was added at 4° C. and the stirred mixture allowed to warm to 20° C. over 40 minutes, then heated to 50° C. for 4 hours and at 20° C. for 3 days. Ammonium chloride solution and ethyl acetate were added and the organic layer dried (sodium sulfate), evaporated and purified by column chromatography using 80% methyl t-butyl ether in hexane to give 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-[[-2-(methylthio)ethyl]amino]-4-(ethylsulfinyl)-1H-pyrazole-3-carbonitrile (0.26 g), m.p.126-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06638956B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-456ae4ad2df34008a073c8d8bf4e9327 |
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| Source note | uspto-grants-2003_10 |
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