Potassium Carbonate → Methyl (6S)-6,8-dihydroxyoctanoate

HRID 370323ノート

反応式

HRID 370323 の反応式
C(=O)([O-])[O-].[K+].[K+].[N+](C1C=CC(C[O:15][C@H:16]([CH2:25][CH2:26][O:27]CC2C=CC([N+]([O-])=O)=CC=2)[CH2:17][CH2:18][CH2:19][CH2:20][C:21]([O:23][CH3:24])=[O:22])=CC=1)([O-])=O>CO>[OH:15][C@H:16]([CH2:25][CH2:26][OH:27])[CH2:17][CH2:18][CH2:19][CH2:20][C:21]([O:23][CH3:24])=[O:22]

参加物

4

実験手順

Under an argon atmosphere, anhydrous potassium carbonate (130 mg, 0.94 mmol) was added to a solution of (6S)-(-)-methyl 6,8-bis(4-nitrobenzoxy)octanoate (461 mg, 0.94 mmol) in methanol (9.4 ml). The mixture was stirred at room temperature for 1 h and quenched with a saturated ammonium chloride solution (50 ml). The mixture was extracted with chloroform (3×50 ml) and the combined organic extracts were washed with brine (50 ml). The organic phase was dried over magnesium sulphate and the solvent was evaporated under reduced pressure to give the crude product which was purified using flash column chromatography with ethyl acetate to give (6S)-(-)-methyl 6,8-dihydroxyoctanoate (147 mg, 82% yield) as a colourless oil. Rf 0.30 (ethyl acetate, 100%).

後処理

  1. customquenched with a saturated ammonium chloride solution (50 ml)
  2. extractionThe mixture was extracted with chloroform (3×50 ml)
  3. washthe combined organic extracts were washed with brine (50 ml)
  4. dry with materialThe organic phase was dried over magnesium sulphate
  5. customthe solvent was evaporated under reduced pressure
  6. customto give the crude product which
  7. customwas purified

出典と根拠

ORDレコード
ord-e5216b6ee0b449ce80262def695c746f
出典データセット
uspto-grants-2000_10
特許番号
US06140512

反応ノート

読み込み中…