HuagongsheHuagongshe Chemistry Print Report · For research reference only
11-Chloro-6,11-dihydrodibenz[b,e]oxepin → HCID 12962149, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 11-Chloro-6,11-dihydrodibenz[b,e]oxepin | HCID 12962148 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 12962149 | HCID 12962149 | 92% |
Reaction Steps
11-Chloro-6,11-dihydrodibenz[b,e]oxepin (32.69 g; 0.14 mole) is dissolved in dry benzene (300 ml) and placed under a dry nitrogen atmosphere. To this solution is added in one portion, CuCN (32.04 g; 0.35 mole). The reaction is heated to reflux for 31/2 hours and filtered while hot. After washing the salts with benzene, the filtrate is removed in vacuo to give a solid. This solid is triturated several times with isopropyl ether and finally hexane to give a solid (92%) of 11-cyano-6,11-dihydrodibenz[b,e]oxepin m.p. 65°-66.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335122 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-561e7c14108a4d719f96242573b9a7d0 |
| Source note | uspto-grants-1982_06 |