反応式
[CH3:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[C:4]([NH:6][C:7]1[CH:15]=[CH:14][C:10]([C:11](O)=[O:12])=[CH:9][CH:8]=1)=[O:5].S(Cl)([Cl:22])=O>>[CH3:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[C:4]([NH:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([Cl:22])=[O:12])=[CH:9][CH:8]=1)=[O:5]参加物
3
実験手順
A mixture of 10.3 g of 4-[(2-methylbenzoyl)amino]benzoic acid and 32 ml of thionyl chloride is refluxed for 1.5 hours. The solution is concentrated in vacuo. Toluene is added and the solvent removed in vacuo. Toluene is added and the mixture chilled and filtered to give the desired product as a yellow solid, 135°-141° C.
後処理
- temperatureis refluxed for 1.5 hours
- concentrationThe solution is concentrated in vacuo
- additionToluene is added
- customthe solvent removed in vacuo
- additionToluene is added
- temperaturethe mixture chilled
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-c6a9d24539574639bdbc2294d2722940
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05733905
関連ノート
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