HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975520Generated: October 28, 2026
Ethyl chloroformate → HCID 10183087, compound
https://huagongshe.com/reaction/975520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 5-Amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrile | HCID 10134900 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10183087 | HCID 10183087 | — |
Reaction Steps
Ethyl chloroformate (1.6 g) was added to a stirred solution of 5-amino-4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole (3.9 g) in pyridine (15 ml). After stirring overnight another addition of ethyl chloroformate (1.0 ml) was made, and the mixture was left for a further 12 hours. The solvent was evaporated in vacuo and the residue was acidified with dilute hydrochloric acid, and extracted with dichloromethane. This extract was washed with water (3×), dried over anhydrous magnesium sulphate, filtered, and evaporated in vacuo. Purification by chromatography on silica (Merck, 40-230 mesh, 0.7 kg cm-2) eluting with ethyl acetate - petroleum ether (1:1) gave a white solid, which was recrystallized from a mixture of dichloromethane and hexane to furnish white crystals of 4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-ethoxycarbonylamino-3-trifluoromethylpyrazole, m.p. 177°-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05608077 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-89de2e51b95448d298cee470c7867d67 |
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| Source note | uspto-grants-1997_03 |
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