HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 5,7-dihydro-6H-dibenz[c,e]azepine-6carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboxamide | HCID 20041714 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5,7-dihydro-6H-dibenz[c,e]azepine-6carbonitrile | HCID 19833886 | — |
Reaction Steps
A mixture of 1.19 g of 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboxamide (see Example 10), 12 ml of chloroform, 2.7 ml of 50% sodium hydroxide solution and 50 mg of triethylamine is stirred at room temperature for 1 hour. The reaction mixture is then poured onto ice/water and the whole is extracted with methylene chloride. The extracts are washed with water, dried over anhydrous sodium sulphate and evaporated, and the residue is purified by flash chromatography on silica gel [eluent: n-hexane/ethyl acetate (9:1)]. There is obtained 5,7-dihydro-6H-dibenz[c,e]azepine-6-carbonitrile, m.p. 118°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04833245 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-a2fecb493a334798b54ea121986c3cf8 |
| Source note | uspto-grants-1989_05 |