Reaktion #1429

ord-bb89d795a1f04c6a9aea5994f10b7016

Reaktionsgleichung

O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
O=C(O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
(S)-2-phthalimido-6-hydroxyhexanoic acid
BrCc1ccccc1
benzyl bromide
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
title product
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
(S)-2-Phthalimido-6-hydroxyhexanoic acid, phenylmethyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mixture was partitioned between ethyl acetate and water
  2. 2
    ExtraktionThe organic extract
  3. 3
    Waschenwas washed with water (twice) and brine
  4. 4
    Trocknendried (sodium sulfate)
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeto give an oil
  7. 7
    Sonstigechromatographed (Merck silica gel, 6/4-ethyl acetate/hexane)
  8. 8
    Sonstigeto give essentially pure product as a solid
  9. 9
    SonstigeRecrystallization from ethyl acetate/hexane
  10. 10
    Sonstigegave 7.173 g

Vorschrift

A slurry of cesium carbonate (3.819 g, 11.7 mmol.) and (S)-2-phthalimido-6-hydroxyhexanoic acid (6.00 g, 21.6 mmol.) in dimethylformamide (60 ml.) was treated with benzyl bromide (3.30 ml., 4.75 g., 27.7 mmol.). After stirring at room temperature for 2 hours, the mixture was partitioned between ethyl acetate and water. The organic extract was washed with water (twice) and brine, then dried (sodium sulfate), filtered and stripped to give an oil. The oil was flash chromatographed (Merck silica gel, 6/4-ethyl acetate/hexane) to give essentially pure product as a solid. Recrystallization from ethyl acetate/hexane gave 7.173 g. (1st crop) and 394 mg. (2nd crop) for a total of 7.567 g. of pure title product; m.p. 106°-108.5° C.; [α]D =-27.5° (c=1.5, methanol). TLC (75/25 ethyl acetate/hexanes) Rf =0.43.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723602uspto-grants-1998_03