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

HRID 2215226Notes

Reaction equation

HRID 2215226 reaction equation
[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]

Participants

4

Procedure

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.

Workup

  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)

Sources & evidence

ORD record
ord-9971a237bddb4b7a9c0a4e8bfc1d5cd7
Source dataset
uspto-grants-2006_09
Patent number
US07109225B2

Reaction notes

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