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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414245Generated: November 2, 2026

Thionyl Chloride → HCID 20368183, compound

https://huagongshe.com/reaction/1414245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantPhosphorus trichlorideHCID 24387—
ReactantPhosphorus tribromideHCID 24614—
ReactantPhosphorus trifluorideHCID 62665—
ReactantHCID 20368169HCID 20368169—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductHCID 20368183HCID 20368183—

Reaction Steps

The haloalkyl imidazolyl pyrazoles, such as 5-amino-1-(haloalkyl)-3-(1-methyl-5-nitro-2-imidazolyl)pyrazole-4-carbonitrile, are prepared by reacting the corresponding hydroxyalkyl compound with a halogenating agent such as phosphorus trichloride, phosphorus tribromide, phosphorus trifluoride, thionyl chloride and the like. Thus, 5-amino-1-(β-hydroxyethyl)-3-(1-methyl-5-nitro-2-imidazolyl)pyrazole-4-carbonitrile, is allowed to react with thionyl chloride in an inert solvent such as benzene, in the presence of a small amount of dimethylformamide to yield 5-amino-1-(β-chloroethyl)-3-(1-methyl-5-nitro-2-imidazolyl)pyrazole-4-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001230
Source datasetuspto-grants-1977_01
ORD IDord-dcddf8eb31f74723896f4d58d4b1f3a0
Source noteuspto-grants-1977_01