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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421502Generated: October 26, 2026

Tert-Butyl nitrite → 3-Cyano-4-(cyclohept-2-enyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole

https://huagongshe.com/reaction/1421502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
Reactant5-Amino-3-cyano-4-(cyclohept-2-enyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoleHCID 9866509—
SolventTetrahydrofuranHCID 8028—
Product3-Cyano-4-(cyclohept-2-enyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazoleHCID 995280040%

Reaction Conditions

Temperature67.5 °C

Reaction Steps

To 5-amino-3-cyano-4-(cyclohept-2-enyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole (208 mg, 0.5 mmol, Example 10) in dry THF (8 ml) heated at 65° C. was added dropwise tert-butyl nitrite (160 mg, 1.5 mmol) in dry THF (2 ml) over 30 min. The solution was heated for a further 2 hr at 65-70° C. The solvent was removed in vacuo and the resulting brown oil purified by silica chromatography (eluting with hexane, hexane/diethyl ether 19/1, hexane/diethyl ether 9/1, hexane/diethyl ether 4/1, hexaneldiethyl ether 1/1, finally diethyl ether). The resulting orange solid was recrystallised from hexane to yield 80 mg of the title compound as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077859
Source datasetuspto-grants-2000_06
ORD IDord-4d0d33439d4f43ec9fca6e440fe780f4
Source noteuspto-grants-2000_06