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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605014Generated: October 30, 2026

Hydrogen iodide → HCID 86733206, compound

https://huagongshe.com/reaction/1605014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen iodideHCID 24841—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86733207HCID 86733207—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 86733206HCID 86733206—

Reaction Steps

Sodium borohydride (76 g, 0.02 mole) is added to a slurry of 1,2-dimethyl-3-(m-fluorophenyl)-5-phenyl-pyrazolinium iodide (4 g, 0.01 mole) in isopropanol (125 ml). After becoming homogeneous, the reaction mixture is stirred for 24 hours. Water (10 ml) is then slowly added. Isopropanol is removed on a rotary evaporator and resultant residue is slurried in water (50 ml) and extracted with chloroform. Evaporation of the organic layer yields an oil, which is slurried in water. Aqueous hydriodic acid (5 ml, 46-50%) is next added. After stirring for one hour, resulting solid is filtered and dried to give 3.3 g, 83%; melting point 187°-189°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03948936
Source datasetuspto-grants-1976_04
ORD IDord-a9b966a062be4e458eb539bd4b5e78fd
Source noteuspto-grants-1976_04