2-[(4-Nitrophenyl)sulfanyl]pyridine → 4-[(Pyridin-2-yl)sulfanyl]aniline
반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=2)=[CH:6][CH:5]=1)([O-])=O>C(O)(=O)C>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[S:10][C:7]1[CH:8]=[CH:9][C:4]([NH2:1])=[CH:5][CH:6]=1참가 물질
3
실험 절차
2-[(4-nitrophenylsulfanyl) pyridine (8.0 g) was dissolved in acetic acid (64 ml), and reduced iron (24 g) was added to the mixture, and then, the mixture was stirred for 16 hours at room temperature. The mixture was filtered with Celite, washed with ethyl acetate, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give 4-(2-pyridinylsulfanyl) aniline (6.3 g).
후처리
- filtrationThe mixture was filtered with Celite
- washwashed with ethyl acetate
- customthe solvent was removed under reduced pressure
- customthe obtained residue was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-30c13dac58ac4403b9d81748d32546b9
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07262185B2
반응 노트
불러오는 중…