반응식
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[CH2:8]([Li])[CH2:9][CH2:10][CH3:11].[CH3:13][N:14](OC)[C:15](OCC)=O.CC[O:24]CC>>[N:4]1[CH:5]=[CH:6][CH:7]=[C:2]([C:8]([C:9]2[CH:13]=[N:14][CH:15]=[CH:11][CH:10]=2)=[O:24])[CH:3]=1참가 물질
실험 절차
To a solution of 3-bromopyridine (9.84 g,0.062 mol) in 300 ml of ether cooled to -78° C. was added n-butyllithium (1.6M, 41 ml, 0.066 mol) and stirred for 30 min. N-Methyl,N-methoxy-urethane (3.76 g, 0.028 mol) in 20 ml of ether was added in 10 min, the mixture was stirred (-78° C.) for 1 h, allowed to warm to room temperature and stirred for 2 h. The reaction mixture was quenched with 6N HCl (100 ml) and stirred. The aqueous layer was basified with 10% NaOH solution, extracted with ethyl acetate (2×) and methylene dichloride. The organic layer was dried over sodium sulfate, concentrated in vacuo, and the residue was purified by chromatography on silica (ethyl acetate, 10% methanol/ethyl acetate) to afford 1,7 g (33%) of di-(3-pyridyl)ketone.
후처리
- stirringthe mixture was stirred (-78° C.) for 1 h
- stirringstirred for 2 h
- customThe reaction mixture was quenched with 6N HCl (100 ml)
- stirringstirred
- extractionextracted with ethyl acetate (2×) and methylene dichloride
- dry with materialThe organic layer was dried over sodium sulfate
- concentrationconcentrated in vacuo
- customthe residue was purified by chromatography on silica (ethyl acetate, 10% methanol/ethyl acetate)
출처 및 근거
- ORD 기록
- ord-f5ddc0c1f9244b348d7959c28e5a8ef7
- 출처 데이터셋
- uspto-grants-1997_02
- 특허 번호
- US05604224
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