2,3-Dichlorophenoxyacetic acid → (2,3-Dichlorophenoxy)acetyl chloride
反応式
[Cl:1][C:2]1[C:12]([Cl:13])=[CH:11][CH:10]=[CH:9][C:3]=1[O:4][CH2:5][C:6](O)=[O:7].S(Cl)([Cl:16])=O>>[Cl:1][C:2]1[C:12]([Cl:13])=[CH:11][CH:10]=[CH:9][C:3]=1[O:4][CH2:5][C:6]([Cl:16])=[O:7]参加物
3
実験手順
After filling in a dry 250 ml flask respectively 59.89 g (0.271 mol) of 2,3-dichlorophenoxyacetic acid synthesized in Example 5 and 79.1 ml (1.084 mol) of thionyl chloride, the reaction mixture was then heated and refluxed for 4-5 hours. When treated as in Example 2 on completion of the reaction, 60.93 g of 2,3-dichlorophenoxyacetyl chloride was obtained as a raw reaction product.
後処理
- customAfter filling in a dry 250 ml flask
- temperaturerefluxed for 4-5 hours
- additionWhen treated as in Example 2 on completion of the reaction
出典と根拠
- ORDレコード
- ord-5c71fef2772d4dc980e163e043f99a3b
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05139564
反応ノート
読み込み中…