2-(Carboxymethyl)-4-chlorobenzoic acid → 156590-23-7
反応式
[Cl:1][C:2]1[CH:11]=[C:6]([CH2:7][C:8]([OH:10])=O)[C:5]([C:12]([OH:14])=[O:13])=[CH:4][CH:3]=1>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:11]=[C:6]2[CH2:7][C:8]([O:14][C:12](=[O:13])[C:5]2=[CH:4][CH:3]=1)=[O:10]参加物
3
実験手順
The starting material is prepared as follows. The mixture of 6.2 g of 5-chlorohomophthalic acid and 70 ml of acetic anhydride is refluxed for 1/2 hour and evaporated. The residue is washed with chloroform, carbon tetrachloride and dryed to yield the 5-chlorohomophthalic anhydride melting at 170°-173°.
後処理
- customThe starting material is prepared
- temperatureis refluxed for 1/2 hour
- customevaporated
- washThe residue is washed with chloroform, carbon tetrachloride
出典と根拠
- ORDレコード
- ord-be8343e6eb8142cba46df08941cf1afc
- 出典データセット
- uspto-grants-1977_05
- 特許番号
- US04025505
反応ノート
読み込み中…