Benzene → HCID 20510805、化合物
反応式
[CH:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.FC(F)(F)C(O[I:12](OC(=O)C(F)(F)F)[C:13]([F:43])([F:42])[C:14]([F:41])([F:40])[C:15]([F:39])([F:38])[C:16]([F:37])([F:36])[C:17]([F:35])([F:34])[C:18]([F:33])([F:32])[C:19]([F:31])([F:30])[C:20]([F:29])([F:28])[C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23])=O.FC(F)(F)C(O)=O.[F:60][C:61]([F:67])([F:66])[S:62]([OH:65])(=[O:64])=[O:63]>>[F:60][C:61]([F:67])([F:66])[S:62]([O-:65])(=[O:64])=[O:63].[F:26][C:21]([F:27])([C:22]([F:23])([F:24])[F:25])[C:20]([F:28])([F:29])[C:19]([F:31])([F:30])[C:18]([F:32])([F:33])[C:17]([F:35])([F:34])[C:16]([F:37])([F:36])[C:15]([F:39])([F:38])[C:14]([F:41])([F:40])[C:13]([F:43])([F:42])[I+:12][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
5
実験手順
0.92 ml (10 mmol) of benzene was added to a mixture of 6.0 g (6.9 mmol) of di(trifluoroacetoxy)iodoheneicosafluoro-n-decane and 32 ml of trifluoroacetic acid under cooling in an ice bath with stirring, and then 0.61 ml (6.9 mmol) of trifluoromethanesulfonic acid was added dropwise thereto. After completion of the addition, the mixture was stirred for 1.5 hours and the solvent was distilled off to obtain a crystalline solid. The solid was washed with hot chloroform to obtain 4.4 g of heneicosafluoro-n-decylphenyliodonium trifluoromethanesulfonate. Yield, 73%. Melting Point 162°-166° C.