HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Difluorobenzonitrile → 2,6-Difluorobenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Difluorobenzonitrile | HCID 74695 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,6-Difluorobenzylamine | HCID 123563 | 94.6% |
Reaction Steps
To an autoclave of 1 l, 150 g of 2,6-difluorobenzonitrile, 150 g of hexane and 7.5 g of Ra—Ni were charged, replacement with hydrogen gas was carried out, and a reaction was carried out at a hydrogen pressure of from 30 to 40 kg/cm2 at a reaction temperature of 130° C. for 2.5 hours. After the completion of the reaction, the reaction mixture was subjected to filtration to separate off the catalyst, and hexane was recovered by distillation, followed by distillation under reduced pressure to obtain 146 g of 2,6-difluorobenzylamine (boiling point: 82° C./25 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06452056B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-7f69a1d21dd24fb38247d9ddf46a466b |
| Source note | uspto-grants-2002_09 |