反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([Cl:11])(Cl)Cl)=[CH:4][CH:3]=1.C(OC(=O)C)(=[O:14])C.S(=O)(=O)(O)[OH:20]>>[C:2]([Cl:1])(=[O:14])[CH3:7].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([Cl:11])=[O:20])=[CH:4][CH:3]=1参加物
5
実験手順
To the reaction residue from run 3 was added 230 g of p-chlorobenzotrichloride, 97 g of acetic anhydride and 2 g of sulfuric acid (98%). The reaction was carried as previously described to give 136 g (91.2%) of acetyl chloride and 177 g (101%) of p-chlorobenzoyl chloride. The average yield from runs 1-4 was 92.7% for acetyl chloride and 93% for p-chlorobenzoyl chloride.
出典と根拠
- ORDレコード
- ord-477d1cc5184141378ebb49a3fc0b2304
- 出典データセット
- uspto-grants-1979_08
- 特許番号
- US04163753
関連ノート
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