反応式
[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]参加物
5
実験手順
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.
後処理
- 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
出典と根拠
- ORDレコード
- ord-cc37459afe1643b99fc32b60888ac2a4
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08629271B2
関連ノート
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