Iodine → 4,5,N-triphenyl-4-isothiazolin-3-one
반응식
[C:1]1([C:7](=[C:17]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[SH:18])[C:8]([NH:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.II.C(N(CC)CC)C>C(Cl)Cl>[C:1]1([C:7]2[C:8](=[O:9])[N:10]([C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)[S:18][C:17]=2[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
실험 절차
A mixture of 150 mg (0.450 mmol) 2,3,N-triphenyl-3-mercaptopropenamide and 25 mL methylene chloride was stirred at room temperature. Added was 115 mg (1 equiv.) of iodine followed by 116 mg (1 equiv.) of triethylamine and the mixture stirred for one hour. Solvent was evaporated and 50 mL ethyl acetate added and the mixture poured into 50 mL water. The organic layer was separated and washed with three 50 mL portions of water. The organic layer was dried, filtered and solvent was evaporated from the filtrate. The resulting solid was recrystallized from ethanol/water to provide 108 mg (0.327 mmol, 73%) 4,5,N-triphenyl-4-isothiazolin-3-one as a tan solid, mp=175°-176° C. NMR (CDCl3 /TMS): 7.30-7.72 (m, 15H). IR (KBr): 1656. Mass spectrum (CI): M/z=330 (M+H)+. Anal. calcd. for C21H15NOS: C 76.57, H 4.59, N 4.25, S 9.73; Found: C 76.25, H 4.40, N 4.19, S 9.81.
후처리
- additionAdded
- stirringthe mixture stirred for one hour
- customSolvent was evaporated
- addition50 mL ethyl acetate added
- additionthe mixture poured into 50 mL water
- customThe organic layer was separated
- washwashed with three 50 mL portions of water
- customThe organic layer was dried
- filtrationfiltered
- customsolvent was evaporated from the filtrate
- customThe resulting solid was recrystallized from ethanol/water
출처 및 근거
- ORD 기록
- ord-c5a340b13279485b9334be581060dcc0
- 출처 데이터셋
- uspto-grants-1995_05
- 특허 번호
- US05411977
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