HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dichlorobenzotrifluoride → [2-Chloro-5-(trifluoromethyl)phenyl]hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dichlorobenzotrifluoride | HCID 9481 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | [2-Chloro-5-(trifluoromethyl)phenyl]hydrazine | HCID 2060249 | — |
| Product | [2-Chloro-4-(trifluoromethyl)phenyl]hydrazine | HCID 2736687 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of 3,4-dichlorobenzotrifluoride (48 g), hydrazine hydrate (65 g) and pyridine (240 g) was stirred and heated at 150° C. for 6 hours in an autoclave at a pressure of 4 bar. The cooled mixture was quenched with sodium hydroxide solution and the organic layer evaporated in vacuo. The residue was dissolved in diethyl ether, washed (water) and the ether evaporated to give 2-chloro-4-trifluoromethylphenylhydrazine and 2-chloro-5-trifluoromethylphenylhydrazine as a 95/5 mixture (36 g),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410737B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-63687c2795ab47eba8505e66b61fc6b6 |
| Source note | uspto-grants-2002_06 |