Ethyl ethoxyacetate → Ethoxymethyl 5-methyl-1,3,4-oxadiazol-2-yl ketone

HRID 406274

反応式

HRID 406274 の反応式
[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

  1. customThe reaction mixture was then quenched with 65 mL of LON HCl
  2. extractionextracted with EtOAc
  3. washThe organic layer was washed with water
  4. dry with materialbrine, dried over anhydrous Na2SO4
  5. concentrationconcentrated
  6. 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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