Thionyl Chloride → HCID 20347860、化合物
反応式
S(Cl)([Cl:3])=O.[C:5]([C:7]1[C:8]([CH3:16])=[C:9]([CH:13]=[CH:14][CH:15]=1)[C:10](O)=[O:11])#[N:6]>>[C:5]([C:7]1[C:8]([CH3:16])=[C:9]([CH:13]=[CH:14][CH:15]=1)[C:10]([Cl:3])=[O:11])#[N:6]参加物
3
実験手順
75 cc of thionyl chloride and 30 g of 3-cyano-2-methyl-benzoic acid [prepared by process in C. R. Acad. Sci., Vol. 235(1952), p. 1660] were refluxed for 11/2 hours and after cooling, excess thionyl chloride was removed under reduced pressure. The last traces of thionyl chloride were removed by addition of benzene and distillation under reduced pressure. The residue was purified by rectification under reduced pressure to obtain 27.4 g of 3-cyano-2-methyl-benzoyl chloride in the form of colorless crystals melting at 62° C.
後処理
- temperatureafter cooling
- customexcess thionyl chloride was removed under reduced pressure
- customThe last traces of thionyl chloride were removed by addition of benzene and distillation under reduced pressure
- customThe residue was purified by rectification under reduced pressure
出典と根拠
- ORDレコード
- ord-bea1d8e8a9cc424cbcc478e2bc6662ef
- 出典データセット
- uspto-grants-1980_03
- 特許番号
- US04192890
反応ノート
読み込み中…