反応式
[CH3:1][C:2]1[O:3][CH:4]=[N:5][N:6]=1.[Li]CCCC.[CH2:12]([O:14][CH2:15][C:16](OCC)=[O:17])[CH3:13]>C1COCC1.C1(C)C=CC=CC=1>[CH3:1][C:2]1[O:3][C:4]([C:16]([CH2:15][O:14][CH2:12][CH3:13])=[O:17])=[N:5][N:6]=1参加物
6
反応条件
- 温度
- -40 °C
実験手順
To a stirred solution of the 2-methyl-1,3,4-oxadiazole (5.0 g, 59.5 mmol) in THF (100 mL) was added dropwise n-BuLi (23.79 mL, 59.5 mmol) in toluene under N2 at −78° C. After 1 h, ethyl ethoxyacetate (10.22 g, 77 mmol) was added. The reaction mixture was then allowed to warm to −40° C. and stirred for 2 h. The reaction mixture was then quenched with 65 mL of LON HCl and extracted with EtOAc. The organic layer was washed with water and then brine, dried over anhydrous Na2SO4, and concentrated. The resulting residue was purified on a flash chromatography column (Biotage™-40M) using a gradient of 0-100% of n-hexane/Et2O to give the desired product. 1H NMR (500 MHz, CD3OD): δ 1.27 (t, 3H), 2.64 (s, 3H), 3.69 (q, 2H), 4.88 (s, 2H).
後処理
- customThe reaction mixture was then quenched with 65 mL of LON HCl
- extractionextracted with EtOAc
- washThe organic layer was washed with water
- dry with materialbrine, dried over anhydrous Na2SO4
- concentrationconcentrated
- customThe resulting residue was purified on a flash chromatography column (Biotage™-40M)
出典と根拠
- ORDレコード
- ord-6fa059c989d04a55b66333cae6dca4f2
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08754099B2
関連ノート
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