HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866399Generated: October 31, 2026
Benzonitrile → Alpha-benzylaminobenzylphosphonic acid
https://huagongshe.com/reaction/866399
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | Alpha-benzylaminobenzylphosphonic acid | HCID 4469578 | — |
Reaction Steps
To a solution of benzonitrile (75g; 0.73 mole) in diethyl phosphite (200g; 1.45 mole) was added W-2 Raney nickel (6g) and the whole mixture charged in an autoclave. The reactor was pressured to 600 psi with hydrogen and the mixture heated to 60° C. The pressure was maintained at 550-600 psi by addition of hydrogen as the reduction proceeded. After 18 hours, uptake of hydrogen had ceased. After cooling hydrogen was released and the catalyst filtered as the reaction product was removed from the reactor. Excess diethyl phosphite and unreacted benzonitrile was removed (135g) by distillation under reduced pressure. The residue was diethyl N-benzylα-aminobenzylphosphonate. Hydrolysis of this residue with 18% HCl after crystallization yielded N-benzylα-amino benzylphosphonic acid, 83g (82%), mp 233°-6°. ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04098849 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-b91e18bd9fce42d38fa775d835135030 |
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| Source note | uspto-grants-1978_07 |
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