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Cyanogen Bromide → 5,7-dihydro-6H-dibenz[c,e]azepine-6carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cyanogen Bromide | HCID 10476 | — |
| 反応物 | 5H-Dibenz(c,e)azepine, 6,7-dihydro- | HCID 81183 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 5,7-dihydro-6H-dibenz[c,e]azepine-6carbonitrile | HCID 19833886 | — |
反応手順
A solution of 1.91 g of cyanogen bromide in 20 ml of chloroform is added dropwise at 5°-10° C. within 25 minutes to a solution, cooled to 5° C., of 7 g of 6,7-dihydro-5H-dibenz[c,e]azepine in 50 ml of chloroform. The reaction mixture is stirred for a further 1 hour and then a small amount of the hydrobromide salt of the still unreacted azepine is filtered off. The filtrate is washed three times with water, dried over anhydrous sodium sulphate and evaporated. There is obtained solid 5,7-dihydro-6H-dibenz[c,e]azepine-6-carbonitrile, m.p. 123°-126° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04766115 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-ec01c07dd42e42d19e85933e8284aee8 |
| 出典メモ | uspto-grants-1988_08 |