反応式
[CH3:1][S:2]([C:5]1[CH:13]=[CH:12][C:8]([C:9](O)=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3].S(Cl)([Cl:16])=O>>[CH3:1][S:2]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([Cl:16])=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3]参加物
3
実験手順
A mixture of 11.2 g (0.056 mol) of p-methylsulfonyl-benzoic acid prepared in Example 4 and 30 ml of thionyl chloride were heated under reflux to give a clear solution. Removal of the excess of thionyl chloride under reduced pressure obtained white solid and without purification put into the next reaction.
後処理
- temperaturewere heated
- temperatureunder reflux
- customto give a clear solution
- customRemoval of the excess of thionyl chloride under reduced pressure
- customobtained white solid
- customwithout purification
- customput into the next reaction
出典と根拠
- ORDレコード
- ord-dc2391ad1b0d413495c6bf541d6f4f16
- 出典データセット
- uspto-grants-2005_11
- 特許番号
- US06960611B2
関連ノート
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