HCID 13645987, 화합물 → HCID 13645989, 화합물
반응식
CC([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Se:15][CH3:16])(=[O:8])=[O:7])(C)C>FC(F)(F)C(O)=O>[CH3:16][Se:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[S:6]([NH2:5])(=[O:8])=[O:7]참가 물질
3
실험 절차
Under nitrogen a solution of N-(1,1-dimethylethyl)-2-(methylselenyl)benzenesulfonamide (34.5 g, 0.113 mmol) in trifluoroacetic acid (100 mL) was stirred at room temperature overnight. The solvent was then rotary evaporated to leave an amber solid. This was again treated with trifluoroacetic acid (100 mL) at room temperature overnight. The mixture was concentrated in vacuo, then poured into ice-water. The solid was collected, rinsed with ice-water, and dried in vacuo. The crude product was recrystallized from hot benzene (5 mL/g), collected at room temperature, rinsed with benzene and hexanes, and dried. The 2-(methylselenyl)benzenesulfonamide (23.1 g) obtained melted at 119°-121° C.
후처리
- customThe solvent was then rotary evaporated
- customto leave an amber solid
- concentrationThe mixture was concentrated in vacuo
- additionpoured into ice-water
- customThe solid was collected
- washrinsed with ice-water
- customdried in vacuo
- customThe crude product was recrystallized from hot benzene (5 mL/g)
- customcollected at room temperature
- washrinsed with benzene and hexanes
- customdried
출처 및 근거
- ORD 기록
- ord-b0c1330bfec44d72ac5e08c6f380ee3e
- 출처 데이터셋
- uspto-grants-1986_05
- 특허 번호
- US04588432
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