Hydrochloric Acid → Ethyl 9,10-dihydrophenanthrene-1-carboxylate
反応式
N[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=[CH:9][C:10]1[CH:20]=[CH:19][CH:18]=[CH:17][C:11]=1[C:12]([O:14][CH2:15][CH3:16])=[O:13].Cl.N([O-])=O.[Na+]>C(O)(=O)C.O.S([O-])([O-])(=O)=O.[Cu+2]>[C:11]1([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:10]2[CH2:9][CH2:8][C:3]3[C:4](=[CH:5][CH:6]=[CH:7][CH:2]=3)[C:20]=2[CH:19]=[CH:18][CH:17]=1参加物
実験手順
To a stirred solution of ethyl 2-[2-(2-aminophenyl)ethenyl]-benzoate (13.5 grams, 0.05 mole) in warm glacial acetic acid (75 ml) was added a solution of concentrated hydrochloric acid (12 ml) in water (10 ml). The mixture was cooled to 0°, and during a 20 minute period a solution of sodium nitrite (3.7 grams, 0.054 mole) in water (30 ml) was added. The resultant mixture was stirred at 0°-5° for three hours. During a 90 minute period the mixturre was added to a refluxing solution of copper sulfate (35 grams, 0.14 mole) in water (500 ml). After complete addition, glacial acetic acid (40 ml) was added and the mixture refluxed for one hour. The mixture was cooled to room temperature and extracted with three 200 ml portions of methylene chloride. The extracts were combined, washed with water, and evaporated under reduced pressure to give a brown oil. Distillation of the oil under reduced pressure gave ethyl 9,10-dihydrophenanthrene-1-carboxylate (5.5 grams, bp 145°-165°/0.25 mm) as a yellow oil.
後処理
- temperatureThe mixture was cooled to 0°
- additionwas added
- temperaturethe mixture refluxed for one hour
- extractionextracted with three 200 ml portions of methylene chloride
- washwashed with water
- customevaporated under reduced pressure
- customto give a brown oil
- distillationDistillation of the oil under reduced pressure
出典と根拠
- ORDレコード
- ord-e3cab5f6bb2248aeaceb4ea173ad0ed0
- 出典データセット
- uspto-grants-1984_02
- 特許番号
- US04433182
反応ノート
読み込み中…