HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzamide | HCID 2331 | 24% |
Reaction Steps
Watanabe, in Bull. Chem. Soc. Japan, 37, 1325 (1964), teaches the conversion of benzonitrile to benzamide with precipitated copper and Urushibara copper (U--Cu). The precipitated copper was prepared from a cupric chloride solution and zinc dust and was reacted with benzonitrile in water for 8 hours to give a 7% yield of benzamide. U--Cu--A was prepared by mixing zinc dust with a solution of cupric chloride and then leaching the resultant product with 13% acetic acid. The reaction of benzonitrile in water with U--Cu--A for 8 hours gave a 24% yield of benzamide with no recovery of benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE031430 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-19df92ef1bb942268027cde2267b593c |
| Source note | uspto-grants-1983_10 |