Phenol → Phenyl 5-bromo-2-hydroxybenzoate
反応式
S(Cl)(Cl)=O.[Br:5][C:6]1[CH:14]=[C:10]([C:11]([OH:13])=[O:12])[C:9]([OH:15])=[CH:8][CH:7]=1.[C:16]1(O)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C1C=CC=CC=1>[Br:5][C:6]1[CH:14]=[C:10]([C:11]([O:13][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:12])[C:9]([OH:15])=[CH:8][CH:7]=1参加物
5
実験手順
80 ml of thionyl chloride was gradually added to a benzene suspension of 217 g of 5-bromosalicyclic acid and 113 g of phenol, followed by refluxing for ten hours under heating. After distilling off the benzene, ice-water was added to the residue, and the precipitate formed was collected by filtration, followed by drying. Yield: 210 g.
後処理
- temperatureby refluxing for ten hours
- temperatureunder heating
- distillationAfter distilling off the benzene, ice-water
- additionwas added to the residue
- customthe precipitate formed
- filtrationwas collected by filtration
- customby drying
出典と根拠
- ORDレコード
- ord-fff0888236b54b86aff40ea01a9b6ec8
- 出典データセット
- uspto-grants-1987_01
- 特許番号
- US04637902
反応ノート
読み込み中…