반응식
[CH2:1]([Li])CCC.[CH2:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1)[CH3:7].CI>O1CCCC1>[CH:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1)([CH3:1])[CH3:7]참가 물질
5
실험 절차
A solution of butyllithium (1.6M in hexanes, 50 mL) was added dropwise over 20 min to a solution of 2-ethylpyridine (9.34 mL) in tetrahydrofuran (50 mL) at −70° C. The mixture was stirred for 2 h then methyl iodide (5 mL) was added dropwise over 15 min. The resulting orange slurry was allowed to warm to RT and stirred overnight. The solvent was evaporated and the residue diluted with diethylether (100 mL). The organic layer was washed with water (2×100 mL) and brine (100 mL), then dried over sodium sulphate, filtered and evaporated to give the subtitled compound as a yellow oil. Yield 9.1 g.
후처리
- stirringstirred overnight
- customThe solvent was evaporated
- additionthe residue diluted with diethylether (100 mL)
- washThe organic layer was washed with water (2×100 mL) and brine (100 mL)
- dry with materialdried over sodium sulphate
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-cc37459afe1643b99fc32b60888ac2a4
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08629271B2
연결된 노트
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