HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 21844481, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-[2-(5-Cyano-2-benzofuranyl)ethyl]benzoic acid | HCID 21844293 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21844481 | HCID 21844481 | 78.5% |
Reaction Steps
At room temperature, 1 g of 4-[2-(5-cyano-2-benzofuranyl)ethyl]benzoic acid and 578 mg of 1-hydroxybenzotriazole were dissolved in 100 ml of dichloromethane, followed by the addition of 780 mg of 1,3-dicyclohexylcarbodiimide and by subsequent stirring at the same temperature for 3 hours. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using a chloroform/ethanol mixture as an elution solvent, and the thus purified product was crystallized from a benzene/n-hexane mixture. In this way, 1.1 g of 2-[2-[4-[[(1-benzotriazolyl)oxy]-carbonyl]phenyl]ethyl]-5-benzofurancarbonitrile was obtained in a powdery form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866577 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-2b3a40c2d52b418db3794ef5b77f16c9 |
| Source note | uspto-grants-1999_02 |