Triethylamine → 4-[[4'-(Octyloxy)-4-biphenylyl]carbonyloxy]benzoic acid 1-(trifluoromethyl)heptyl ester
反応式
[OH:1][C:2]1[CH:21]=[CH:20][C:5]([C:6]([O:8][CH:9]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[C:10]([F:13])([F:12])[F:11])=[O:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.[CH2:29]([O:37][C:38]1[CH:43]=[CH:42][C:41]([C:44]2[CH:49]=[CH:48][C:47]([C:50](Cl)=[O:51])=[CH:46][CH:45]=2)=[CH:40][CH:39]=1)[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]>C(Cl)Cl.O>[CH2:29]([O:37][C:38]1[CH:43]=[CH:42][C:41]([C:44]2[CH:49]=[CH:48][C:47]([C:50]([O:1][C:2]3[CH:3]=[CH:4][C:5]([C:6]([O:8][CH:9]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[C:10]([F:11])([F:12])[F:13])=[O:7])=[CH:20][CH:21]=3)=[O:51])=[CH:46][CH:45]=2)=[CH:40][CH:39]=1)[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]参加物
実験手順
To a mixture of the 1,1,1-trifluoro-2-octyl 4-hydroxybenzoate prepared above (0.53 g) and triethylamine (0.18 g) in methylene chloride (10 ml) was slowly added under ice cooling a solution of 4-n-octyloxybiphenyl-4'-carboxylic acid chloride (0.73 g) in methylene chloride (10 ml). After the mixture was left to stand until it reached room temperature, it was stirred overnight. The mixture was poured in water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water, in this order, and dehydrated over anhydrous magnesium sulfate. After the solution was distilled under reduced pressure to remove the solvent, the residue was purified by silica-gel column chromatography to obtain the titled compound (0.4 g, [α]D20 =+32.2).
後処理
- waitAfter the mixture was left
- customreached room temperature
- extractionextracted with methylene chloride
- washThe extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water, in this order
- distillationAfter the solution was distilled under reduced pressure
- customto remove the solvent
- customthe residue was purified by silica-gel column chromatography
出典と根拠
- ORDレコード
- ord-2fdd760dab554777912ece06e6a7aac2
- 出典データセット
- uspto-grants-1994_07
- 特許番号
- US05328641
反応ノート
読み込み中…