Methanol → 5-Methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one

HRID 41683

反応式

HRID 41683 の反応式
[CH:1]12[O:10][CH:7]([CH2:8][CH2:9]1)[CH:6]1[CH:2]2[C:3](=[O:12])[CH2:4][C:5]1=[O:11].[CH3:13]O>[Na+].Cl[Au-](Cl)(Cl)Cl>[CH3:13][O:12][C:3]1[CH:2]2[CH:6]([CH:7]3[O:10][CH:1]2[CH2:9][CH2:8]3)[C:5](=[O:11])[CH:4]=1

参加物

4

反応条件

温度
60 °C

実験手順

To a suspension of 10-oxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione (9.97 g, 60 mmol) in methanol (200 ml) is added sodium tetrachloroaurate (597 mg, 1.5 mmol) and the reaction mixture is heated to 60° C. for 7 hours. The reaction mixture is allowed to cool down to room temperature and left to stand overnight. The reaction mixture is concentrated under reduced pressure, dissolved in ethyl acetate (200 ml) and washed with aqueous 2N sodium carbonate (100 ml), followed by saturated brine (100 ml). The organic layer is then dried over magnesium sulphate and concentrated under reduced pressure to give 5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (8.62 g)

後処理

  1. temperatureto cool down to room temperature
  2. waitleft
  3. concentrationThe reaction mixture is concentrated under reduced pressure
  4. dissolutiondissolved in ethyl acetate (200 ml)
  5. washwashed with aqueous 2N sodium carbonate (100 ml)
  6. dry with materialThe organic layer is then dried over magnesium sulphate
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-0037591a615e4fe095b275a6c05ed8ab
出典データセット
uspto-grants-2013_09
特許番号
US08530667B2

関連ノート

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