HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34274Generated: October 26, 2026
3,5-Difluorobenzonitrile → 3,5-Difluorobenzylamine
https://huagongshe.com/reaction/34274
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Difluorobenzonitrile | HCID 587204 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,5-Difluorobenzylamine | HCID 145211 | — |
Reaction Steps
A mixture of 3,5-difluorobenzonitrile (13.9 g., 0.10 mole) in methanol [(140 ml.), saturated with ammonia]and Raney nickel was shaken under hydrogen (50 psi.) for 1.5 hours and the solution was decanted from the catalyst. The solution was filtered, evaporated to an oil, and dissolved in ethyl acetate. The ethyl acetate solution was extracted twice with 1N HCl (75 ml.) and the aqueous solution was washed once with ethyl acetate, made basic with 10% sodium hydroxide, and extracted with three portions of ethyl acetate (100 ml.). The ethyl acetate solution was washed with water and brine, dried, and the solvent removed under vacuum. The residue was diluted with ether, filtered, and the solvent was removed under vacuum to give 3,5-difluorobenzylamine as an oil (11.7 g., 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04761415 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-0d11a5a0ac9547fa97c644a1d78afa6d |
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| Source note | uspto-grants-1988_08 |
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