HCID 54135524、化合物 → HCID 21520541、化合物
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:15]3[C:10](=[CH:11][CH:12]=[C:13]([C:18](C)([C:22](O)=O)[C:19]([OH:21])=[O:20])[CH:14]=3)[N:9]=2)=[CH:4][CH:3]=1>C(OCC)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:15]3[C:10](=[CH:11][CH:12]=[C:13]([CH:18]([CH3:22])[C:19]([OH:21])=[O:20])[CH:14]=3)[N:9]=2)=[CH:4][CH:3]=1参加物
3
実験手順
10 g of 2-(p-chlorophenyl)-α-methyl-6-quinolinemalonic acid are heated to 190°C for 20 minutes. The melt is cooled and dissolved in ethyl acetate, and the solution is extracted with 0.5 N sodium carbonate solution. The sodium carbonate extracts are adjusted to pH 5 and extracted with ethyl acetate. The ethyl acetate extracts, on evaporation and recrystallisation of the residue from ethyl acetate-petroleum ether, yield 2-(p-chlorphenyl)-α-methyl-6-quinolineacetic acid of melting point 188°-189°C.
後処理
- temperatureThe melt is cooled
- extractionthe solution is extracted with 0.5 N sodium carbonate solution
- extractionextracted with ethyl acetate
- customThe ethyl acetate extracts, on evaporation and recrystallisation of the residue from ethyl acetate-petroleum ether
出典と根拠
- ORDレコード
- ord-ce5c56daa02246ee93fabe4fb82cb8bb
- 出典データセット
- uspto-grants-1976_08
- 特許番号
- US03973022
反応ノート
読み込み中…