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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720457Generated: November 3, 2026

Hydrochloric Acid → HCID 22418338, compound

https://huagongshe.com/reaction/1720457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcrylonitrileHCID 7855—
ReactantTert-Butyl nitriteHCID 10906—
ReactantHCID 22418358HCID 22418358—
SolventAcetonitrileHCID 6342—
ProductHCID 22418338HCID 2241833869%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2.90 g (21.6 mmoles) of cupric chloride in a mixture of 20 mL of acetonitrile and 40 mL of acrylonitrile was added 2.73 mL (2.37 g, 23.0 mmoles) of t-butyl nitrite. The resulting black solution was cooled to 0° C., and a solution of 6.66 g (14.7 mmoles) of 1-(2,6-dichloro-4-trifluoromethylphenyl)-2-amino-3-trifluoromethylthio-4-cyano-5-chloropyrrole prepared according to EXAMPLE 8 in 25 mL of acetonitrile was added dropwise and with stirring over a period of 20 minutes. The mixture was allowed to stir for 4 hours at room temperature and was then poured into 400 mL of 1N aqueous HCl and partitioned successively with dichloromethane and water. The organic extracts were dried over anydrous MgSO4 and concentrated. The residual brown oil was chromatographed on silica gel eluting initially with 2:1 and then 1:1 v/v dichloromethane-hexane to give 5.30 g (69%) of 1 -(2,6-dichloro-4-trifluoromethylphenyl)-2-(2-chloro-2-cyanoethyl)-3-trifluoromethylthio-4-cyano-5-chloropyrrole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506260
Source datasetuspto-grants-1996_04
ORD IDord-193cdadd30084dda8a82f2f94a652ec1
Source noteuspto-grants-1996_04