HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-Allyl-1-phenyl-2-(3-sulfamoyl-4-chlorobenzoyl)-hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 1-Phenyl-2-(3-sulfamoyl-4-chlorobenzoyl)-hydrazine | HCID 15571501 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Allyl-1-phenyl-2-(3-sulfamoyl-4-chlorobenzoyl)-hydrazine | HCID 15571502 | — |
Reaction Steps
In a three necked 12 liter round bottom reaction flask equipped with a mechanical stirrer and reflux condenser was placed isopropanol 6.1 liters and 1-phenyl-2-(3-sulfamoyl-4-chlorobenzoyl)-hydrazine 1.3 kg (4.1 mol), potassium iodide 68.0 g (0.41 mol) and allyl bromide 768 g (8 mol). This mixture was stirred at gentle reflux for about 20 hours then suction filtered while still hot. The cake was washed with isopropanol 300 ml and the combined filtrate and wash were diluted with warm water 2.7 liters. Crystallization occured in about 0.5 hours. The crystals were filtered and washed with isopropanol-water (70% v/v) to provide the compound (m.p. 99°-101° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04258059 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-8daef974bced459fb9a7bad44996d53f |
| Source note | uspto-grants-1981_03 |