HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen iodide → HCID 86733206, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86733207 | HCID 86733207 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86733206 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03948936 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-a9b966a062be4e458eb539bd4b5e78fd |
| Source note | uspto-grants-1976_04 |