Hydrochloric Acid → Benzamide, 2-(benzoyloxy)-N-(4-(benzoyloxy)-3,5-dichlorophenyl)-
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:15]=[C:16]([Cl:19])[C:17]=1[OH:18])[NH:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[OH:13].[C:20](Cl)(=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.Cl>N1C=CC=CC=1>[C:20]([O:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[C:6]([NH:5][C:4]1[CH:3]=[C:2]([Cl:1])[C:17]([O:18][C:6](=[O:14])[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[C:16]([Cl:19])[CH:15]=1)=[O:14])(=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1参加物
実験手順
3',5'-Dichloro-2,4'-dihydroxybenzanilide (1 g.) was dissolved in dry pyridine (15 ml.) in the cold at 0°- 5° C. and to it was added dropwise benzoyl chloride (1.2 ml.). With gentle stirring reaction was continued for several hours. The solution was then poured into ice-cold water and acidified with 1 N hydrochloric acid to pH 2, yielding oily material which was extracted by ethyl acetate. The ethyl acetate solution was washed with 1 N hydrochloric acid and 5% sodium bicarbonate solution in that order and dried with anhydrous sodium sulfate, followed by removal of the solvent by evaporation. The residue was subjected to recrystallization from ether and petroleum ether mixture to give white crystals (1.5 g.) of 2,4'-dibenzoyloxy-3',5'-dichlorobenzanilide. Yield: 88.2%. Melting point: 157°-160° C.
後処理
- customreaction
- waitwas continued for several hours
- additionThe solution was then poured into ice-cold water
- customyielding oily material which
- extractionwas extracted by ethyl acetate
- washThe ethyl acetate solution was washed with 1 N hydrochloric acid and 5% sodium bicarbonate solution in that order
- dry with materialdried with anhydrous sodium sulfate
- customfollowed by removal of the solvent by evaporation
- customThe residue was subjected to recrystallization from ether and petroleum ether mixture
出典と根拠
- ORDレコード
- ord-d02f8d5cd56b4eb1827fed8f2103a123
- 出典データセット
- uspto-grants-1976_08
- 特許番号
- US03973038
反応ノート
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