Sodium Methoxide → o-Phenylbenzoic acid
反応式
Cl[C:2]1[CH:3]=[C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:6][CH:7]=1.Cl[C:20]1[CH2:25][CH2:24][C:23]([C:26]([O:28]CC)=[O:27])=[C:22]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:21]=1.C[O-].[Na+]>CO>[C:13]1([C:4]2[CH:3]=[CH:2][CH:7]=[CH:6][C:5]=2[C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1.[C:31]1([C:22]2[CH:21]=[CH:20][CH:25]=[CH:24][C:23]=2[C:26]([OH:28])=[O:27])[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1参加物
実験手順
To a stirred solution of a mixture(620 mg, 2.54 mmol) of ethyl 4-chloro-2-phenylcyclohexa-2,4-dienecarboxylate and ethyl 4-chloro-2-phenylcyclohexa-1,3-dienecarboxylate in MeOH(5 ml), NaOMe(28% in MeOH, 1.98 g, 10.1 mmol) was added. After stirring for 17 hr at room temperature, the solvent was evaporated under reduced pressure. Water was added to the residue and dil. HCl aq., and it was extracted with AcOEt. The organic layer was washed with brine and dried over MgSO4. After removal of the solvent, the residue was purified by column chromatography on silica gel with n-hexane-AcOEt to afford 136 mg of ethyl 2-phenylbenzoate(y=23.7%) and 236 mg of 2-phenylbenzoic acid(y=53.8%). 1H-NMR(ppm, 300 MHz, CDCl3) δ ester 7.82(1H, dd, J=1.4 and 7.7 Hz), 7.10-7.60(8H), 4.08(2H, d, J=7.0 Hz), 0.98(3H, t, J=7.0 Hz); acid 7.95(1H, d, J=7.9 Hz).
後処理
- customthe solvent was evaporated under reduced pressure
- additionWater was added to the residue and dil. HCl aq., and it
- extractionwas extracted with AcOEt
- washThe organic layer was washed with brine
- dry with materialdried over MgSO4
- customAfter removal of the solvent
- customthe residue was purified by column chromatography on silica gel with n-hexane-AcOEt
出典と根拠
- ORDレコード
- ord-ff111a659b9b44959a78918df1ff6e7d
- 出典データセット
- uspto-grants-2002_01
- 特許番号
- US06340772B1
反応ノート
読み込み中…