Acetic Anhydride → 4-[3-(3-Acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoic acid
反応式
[C:1]([C:4]1[CH:24]=[CH:23][C:7]([O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]2[CH:21]=[CH:20][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=2[Br:22])=[C:6]([CH2:25][CH2:26][CH3:27])[C:5]=1[OH:28])(=[O:3])[CH3:2].[C:29](OC(=O)C)(=[O:31])[CH3:30]>N1C=CC=CC=1>[C:29]([O:28][C:5]1[C:6]([CH2:25][CH2:26][CH3:27])=[C:7]([CH:23]=[CH:24][C:4]=1[C:1](=[O:3])[CH3:2])[O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=1[Br:22])(=[O:31])[CH3:30]参加物
実験手順
In a mixture of pyridine (10 ml) and acetic anhydride (10 ml) was dissolved 4-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-3-bromobenzoic acid (2 g). The solution was heated at 100° to 120° C. for 14 hours, which was then concentrated. The residue was dissolved in chloroform. The solution was washed with dilute hydrochloride acid, which was then dried on sodium sulfate. From the resultant was removed the solvent by evaporation, and the residue was chromatographed on a column of silica gel. Elution was conducted with hexane-ethyl acetate (3:1), (2:1), (1:1) and ethyl acetate in that order. Ethyl acetate fractions were combined and concentrated. The residue was crystallized from chloroform-hexane to give 4-[3-(3-acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoic acid (1.0 g), m.p. 155°-156° C.
後処理
- temperatureThe solution was heated at 100° to 120° C. for 14 hours
- concentrationwhich was then concentrated
- dissolutionThe residue was dissolved in chloroform
- washThe solution was washed with dilute hydrochloride acid, which
- customwas then dried on sodium sulfate
- customFrom the resultant was removed the solvent
- customby evaporation
- customthe residue was chromatographed on a column of silica gel
- washElution
- concentrationconcentrated
- customThe residue was crystallized from chloroform-hexane
出典と根拠
- ORDレコード
- ord-732ff6876d04499a85438c2731c1d17d
- 出典データセット
- uspto-grants-1987_12
- 特許番号
- US04714774
反応ノート
読み込み中…