HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → N-(4-methylfurazan-3-yl)cyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | 3-Amino-4-methylfurazan | HCID 28674 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(4-methylfurazan-3-yl)cyclopropanecarboxamide | HCID 20197118 | — |
Reaction Steps
5 g (about 0.05 moles) of 4-methyl-3-aminofurazan, 50 ml of ethyl ether and 4 ml of pyridine are then loaded into a 100 ml glass reactor. This is cooled to a temperature of from 0° to 10° C. and 5 ml (0.06 moles) of the chloride of cyclopropanecarboxylic acid are added under agitation. Heating is then carried out under reflux for about one hour. After cooling of the reaction mass, the ether is evaporated and the residual solid is transferred into about 100 ml of water. Slight heating is effected for about 30 minutes and then the mass is cooled and filtered, the solid being washed with water. The solid obtained is dried in an oven at 90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04671818 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-6e1ecb825e39456ea89633c4f4a20720 |
| Source note | uspto-grants-1987_06 |