Thionyl Chloride → Monopropyl Terephthaloyl Chloride
反応式
[CH3:1][C:2]1[CH:10]=[C:9]([C:11]([Cl:13])=[O:12])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:6])=[O:5].[C:14](OCCC)(=O)[C:15]1C=CC(C([O-])=O)=CC=1.[K+].S(Cl)(Cl)=O>C1(C)C=CC=CC=1>[CH2:1]([C:2]1[CH:10]=[C:9]([C:11]([Cl:13])=[O:12])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:6])=[O:5])[CH2:14][CH3:15]参加物
5
実験手順
This compound was prepared by the procedure described for monomethyl terephthaloyl chloride. Typical reagent levels were as follows: potassium monopropyl terephthalate (49.0g, 0.20 mole), thionyl chloride (29.8g, 0.25 mole) and 100 ml of toluene. The product was used without further purification.
後処理
- customThis compound was prepared by the procedure
- customThe product was used without further purification
出典と根拠
- ORDレコード
- ord-ac7eb9e4db084883b32afbccc60fb5aa
- 出典データセット
- uspto-grants-1992_01
- 特許番号
- US05078907
反応ノート
読み込み中…