Chlorosuccinimide → 2-Chloro-4-dodecylsulfonylaniline
反応式
[CH2:1]([S:13]([C:16]1[CH:22]=[CH:21][C:19]([NH2:20])=[CH:18][CH:17]=1)(=[O:15])=[O:14])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[Cl:23]N1C(=O)CCC1=O>ClCCCl>[Cl:23][C:21]1[CH:22]=[C:16]([S:13]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])(=[O:15])=[O:14])[CH:17]=[CH:18][C:19]=1[NH2:20]参加物
4
実験手順
A mixture of 4-dodecylsulphonylaniline (519.8 g, 1.6 moles), 1,2-dichlorethane (2.5 liters) and N-chlorosuccinimide (NCS) (110 g, 0.825 moles) was stirred at reflux for 45 minutes, then a further 60 g (0.45 moles) of NCS added. Refluxing was continued for another 45 minutes and another 53 g of NCS was added. The mixture was refluxed for another hour. The total amount of NCS used was 223 g (1.67 moles). TLC showed no starting material. The solvent was removed on the rotavapor, the residue dissolved in ethyl acetate (2 liters), washed with 3×1.5 liters of hot water, dried (MgSO4) and the solvent removed. The product was recrystallized twice from petroleum ether plus a little ethyl acetate to give 513.6 g (89%).