Sodium Methoxide → (2S,3R)-3-(4-benzyloxy-2-ethyl-phenyl)-2-ethoxy-3-hydroxy-propionic acid methyl ester

HRID 2215226ノート

反応式

HRID 2215226 の反応式
[CH3:1][O-:2].[Na+].C([C@H]1COC(=O)N1[C:17](=[O:40])[C@@H:18]([O:37][CH2:38][CH3:39])[C@@H:19]([C:21]1[CH:26]=[CH:25][C:24]([O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[CH:23][C:22]=1[CH2:35][CH3:36])[OH:20])C1C=CC=CC=1>CO>[CH3:1][O:2][C:17](=[O:40])[C@@H:18]([O:37][CH2:38][CH3:39])[C@@H:19]([C:21]1[CH:26]=[CH:25][C:24]([O:27][CH2:28][C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)=[CH:23][C:22]=1[CH2:35][CH3:36])[OH:20]

参加物

4

実験手順

A 5.4 M solution of sodium methoxide (640 μl, 3.5 mmol) was added to an ice-cooled and stirred suspension of (S)-4-benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-ethyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one (1.58 g, 3.1 mmol) in dry methanol (9 ml). The mixture was stirred at 0° C. for 15 min, quenched and neutralized by the addition of dilute aqueous hydrochloric acid (1.0 M). The solution was concentrated under reduced pressure and the residue dissolved in ice water/ethyl acetate 1/1. The layers were separated and the aqueous layer was extracted two times with ethyl acetate. The combined organic layers were washed with ice water and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, cyclohexane/AcOEt) to give 730 mg (2.0 mmol, 65%) of the title compound as colorless liquid. According to 1H-NMR spectroscopy, one single diastereomer was obtained.

後処理

  1. temperaturecooled
  2. stirringThe mixture was stirred at 0° C. for 15 min
  3. customquenched
  4. additionneutralized by the addition of dilute aqueous hydrochloric acid (1.0 M)
  5. concentrationThe solution was concentrated under reduced pressure
  6. dissolutionthe residue dissolved in ice water/ethyl acetate 1/1
  7. customThe layers were separated
  8. extractionthe aqueous layer was extracted two times with ethyl acetate
  9. washThe combined organic layers were washed with ice water
  10. dry with materialdried over sodium sulfate
  11. customThe solvent was removed under reduced pressure
  12. customthe residue purified by column chromatography (silica gel, cyclohexane/AcOEt)

出典と根拠

ORDレコード
ord-9971a237bddb4b7a9c0a4e8bfc1d5cd7
出典データセット
uspto-grants-2006_09
特許番号
US07109225B2

反応ノート

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