Benzaldehyde → HCID 54515570、化合物
反応式
[CH3:1][O:2][C:3]1[C:8]([CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12])=[CH:7][N:6]=[C:5]([CH3:14])[CH:4]=1.[CH:15](=O)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(OC(=O)C)(=O)C>[CH:14]([C:5]1[CH:4]=[C:3]([O:2][CH3:1])[C:8]([CH2:9][CH2:10][CH:11]([CH3:12])[CH3:13])=[CH:7][N:6]=1)=[CH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1参加物
4
実験手順
The starting substance can be manufactured by dissolving 26 g of 4-methoxy-5-isoamyl-2-picoline in 78 ml of benzaldehyde and 86 ml of acetic anhydride and heating the reaction mixture for 16 hours under reflux. After cooling, the mixture is evaporated, treated with 2 N sodium hydroxide solution and extracted with ether. Distillation of the ether residue in a bulb tube in a high vacuum at a temperature of 180°-200° yields 2-styryl-4-methoxy-5-isoamyl-pyridine.
後処理
- temperatureheating the reaction mixture for 16 hours
- temperatureunder reflux
- temperatureAfter cooling
- customthe mixture is evaporated
- additiontreated with 2 N sodium hydroxide solution
- extractionextracted with ether
- distillationDistillation of the ether residue in a bulb tube in a high vacuum at a temperature of 180°-200°
出典と根拠
- ORDレコード
- ord-6fb68f802dee4b79ab26f5ab3b91ed6b
- 出典データセット
- uspto-grants-1976_12
- 特許番号
- US03998955
反応ノート
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