Methanesulfonic Acid → Tris-(4-t-butylphenyl)sulfonium methane sulfonate
반응식
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([C:13]2[CH:18]=[CH:17][C:16]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:15][CH:14]=2)=O)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[C:23]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)([CH3:26])([CH3:25])[CH3:24].[CH3:33][S:34]([OH:37])(=[O:36])=[O:35]>O>[CH3:33][S:34]([O-:37])(=[O:36])=[O:35].[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S+:11]([C:30]2[CH:31]=[CH:32][C:27]([C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:28][CH:29]=2)[C:13]2[CH:18]=[CH:17][C:16]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:15][CH:14]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]참가 물질
5
반응 조건
- 온도
- 100 °C
실험 절차
A mixture of 3 g of bis-(4-t-butylphenyl)sulfoxide, 30 ml of t-butylbenzene and 9.17 g of methane sulfonic acid was heated at 100° C. for 24 hours. The mixture was poured into 100 ml of water and extracted with four 50-ml portions of ether followed by five 50-ml portions of chloroform. The chloroform extracts were dried and the chloroform removed on a rotary evaporator to give 1.03 g of tris-(4-t-butylphenyl)sulfonium methane sulfonate (20.6 percent yield).
후처리
- extractionextracted with four 50-ml portions of ether
- dry with materialThe chloroform extracts were dried
- customthe chloroform removed on a rotary evaporator
출처 및 근거
- ORD 기록
- ord-54db27da258447b6a9fbee5ecc6f4f00
- 출처 데이터셋
- uspto-grants-1984_05
- 특허 번호
- US04451409
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