Benzene → Acetyl chloride, 2,2'-[1,2-phenylenebis(oxy)]bis-
反応式
[C:1]([Cl:6])(=[O:5])[C:2](Cl)=[O:3].[CH:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>>[Cl:6][C:1]([CH2:2][O:3][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:3][CH2:2][C:1]([Cl:6])=[O:5])=[O:5]参加物
3
実験手順
30 g. Of the above acid are added to a mixture of 200 ml. anhydrous benzene. Then 35 g. oxalylchloride are added, the flask being protected by a calcium chloride tube. The mixture is stirred for four days and the diacid progressively dissolves as it is being transformed into the corresponding dichloride. The solution is then evaporated to dryness (without heating) leaving a brownish solid residue which is recrystallized from a mixture of chloroform-benzene giving white crystals.
後処理
- additionOf the above acid are added to a mixture of 200 ml
- customthe flask being protected by a calcium chloride tube
- customThe solution is then evaporated to dryness (without heating)
- customleaving a brownish solid residue which
- customis recrystallized from a mixture of chloroform-benzene giving white crystals
出典と根拠
- ORDレコード
- ord-e8269324f1e94e6aa493aaf3bff55fa8
- 出典データセット
- uspto-grants-1976_06
- 特許番号
- US03966766
反応ノート
読み込み中…