HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 3-cyano-N-[4-(benzoylamino)-benzyl]-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-cyano-N-(4-amino-benzyl)-benzamide | HCID 60893168 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-cyano-N-[4-(benzoylamino)-benzyl]-benzamide | HCID 69308621 | — |
Reaction Steps
A solution of 0.6 g (4.2 mmol) of benzoylchloride in 10 ml of methylene chloride is added dropwise to a solution of 1 g (4 mmol) of 3-cyano-N-(4-amino-benzyl)-benzamide and 0.6 g (6 mmol) of triethylamine in 30 ml of methylene chloride at ambient temperature. After 8 hours at ambient temperature the product which has crystallised out is dissolved in methylene chloride and methanol. After extraction with water the combined organic extracts are dried and evaporated down.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425641B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-2bed51339cdf4881b929757cb7991d35 |
| Source note | uspto-grants-2008_09 |