Nitric Acid → HCID 178512746, 화합물
반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[N+:10]([O-:13])([OH:12])=[O:11].[NH2:14][NH:15][C:16]([NH2:19])=[N:17][NH2:18].[N+]([O-])(O)=O>C(O)C.O>[N+:10]([O-:13])([OH:12])=[O:11].[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[N:18][NH:17][C:16]([NH:15][N:14]=[CH:6][C:5]2[CH:8]=[CH:9][C:2]([Br:1])=[CH:3][CH:4]=2)=[NH:19])=[CH:4][CH:3]=1참가 물질
6
실험 절차
A boiling solution of 20.0 grams of 4-bromobenzaldehyde in 250 milliliters of ethanol is stirred vigorously as a solution of 6.1 grams of 1,2-diaminoguanidine nitrate and 0.5 milliliters of concentrated nitric acid in 50 milliliters of water is added in one portion. The reaction mixture is stirred as the temperature recedes to room temperature. The reaction mixture is allowed to stand for several hours. The precipitate which forms is collected, washed with hot ethanol, air dried and finally dried at 60°C. under reduced pressure. The yield is 16.5 grams of product and the melting point is 178°-180°C. with decomposition.
후처리
- additionis added in one portion
- customrecedes to room temperature
- waitto stand for several hours
- customThe precipitate which forms is collected
- washwashed with hot ethanol, air
- customdried
- customfinally dried at 60°C. under reduced pressure
출처 및 근거
- ORD 기록
- ord-214e1ee5d3cd4e8798a81ae16a992cc6
- 출처 데이터셋
- uspto-grants-1976_03
- 특허 번호
- US03941825
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