Water → Ethyl 2-(bicyclo[3.2.1]octan-3-ylidene)acetate

HRID 1853431ノート

反応式

HRID 1853431 の反応式
[H-].[Na+].[CH3:3][CH2:4][O:5][C:6]([CH2:8]P(OCC)(OCC)=O)=[O:7].[CH:17]12[CH2:24][CH:21]([CH2:22][CH2:23]1)[CH2:20][C:19](=O)[CH2:18]2.O>COCCOC>[CH:17]12[CH2:24][CH:21]([CH2:22][CH2:23]1)[CH2:20][C:19](=[CH:8][C:6]([O:5][CH2:4][CH3:3])=[O:7])[CH2:18]2

参加物

6

反応条件

温度
0 °C

実験手順

To a suspension of NaH (1.55 g, 38.7 mmol, 60% dispersion in oil) in 1,2-dimethoxy ethane (70 mL) at 0° C., triethyl phosphono acetate (8.38 mL, 41.9 mmol) was added. The resulting mixture was stirred 15 minutes at 0° C., 15 minutes at room temperature, and cooled to 0° C. Then, a solution of bicyclo[3.2.1]octan-3-one (Biogene, 4.0 g, 32.2 mmol) in 1,2-dimethoxy ethane (20 mL) was added and the resulting solution was stirred for 5 minutes at 0° C. and then stirred at room temperature overnight. Water was added and the aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with H2O (50 mL), brine (50 mL), dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography using an Analogix® Intelliflash280™ (Hex-EtOAc, 0 to 25%) to give the title compound. MS (DCI/NH3) m/z 212 (M+NH4)+

後処理

  1. temperaturecooled to 0° C
  2. stirringthe resulting solution was stirred for 5 minutes at 0° C.
  3. stirringstirred at room temperature overnight
  4. extractionthe aqueous layer was extracted with ethyl acetate (3×50 mL)
  5. washThe combined organic layers were washed with H2O (50 mL), brine (50 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-ccb359757e2f462a8d4ac6847b39e2e2
出典データセット
uspto-grants-2015_02
特許番号
US08962639B2

反応ノート

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