HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 21418271, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 53778394 | HCID 53778394 | — |
| Product | HCID 21418271 | HCID 21418271 | 95% |
Reaction Steps
1.0 g of 5-chloro-3-p-chlorophenyl-1-phenyl-pyrazole-4-acetonitrile, 10 ml of ethanol and 1.4 g of sodium hydroxide are heated at boiling point for 4 hours until the evolution of ammonia is terminated. The alcohol is distilled in vacuo, treated with ether, purified with active charcoal and the aqueous phase is acidified with hydrochloric acid to pH 3. With a yield of 95 % 5-chloro-3-p-chlorophenyl-1-phenyl-pyrazole-4-acetic acid is obtained; F 179.5°-181°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03974176 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-70d727e7db824a46ae426a8935f1bc2f |
| Source note | uspto-grants-1976_08 |