Réaction #1345

ord-bcfe7e4ce5914fd798eabd94aed3d84f

Équation de réaction

CCOC(=O)CC(=O)CCl
ethyl 4-chloroacetoacetate
CC1(C)OCC(CO)O1
2,2-dimethyl-[1,3]dioxolane-4-methanol
[H-].[Na+]
sodium hydride
CCOC(=O)CC(=O)COCC1COC(C)(C)O1
title compound
Rendement 50.1%
CCOC(=O)CC(=O)COCC1COC(C)(C)O1
4-(2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxy)-3-oxo-butyric acid ethyl ester
Rendement 50.1%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe resulting mixture was cooled in an ice bath
  2. 2
    AutreThe reaction mixture was then quenched with water (100 mL) and tetrahydrofuran
  3. 3
    Autrewas removed under reduced pressure
  4. 4
    ExtractionThe aqueous phase was extracted with ethyl acetate (3×250 mL)
  5. 5
    SéchageThe combined organic fractions was dried (sodium sulfate)
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated in vacuo
  8. 8
    AutreThe residue was purified by flash chromatography on silica gel (grade 9385, Merck, 230-400 mesh, 60 Å)
  9. 9
    workup.ADDITIONa mixture of hexane and ethyl acetate (9:1 and 8:2

Mode opératoire

To a suspension of sodium hydride (55 g, 60% dispersion in oil) in tetrahydrofuran (1L) under a nitrogen atmosphere was added a solution of 2,2-dimethyl-[1,3]dioxolane-4-methanol (XV, 102.4 g) in tetrahydrofuran (250 mL) over 15 min at room temperature. The resulting mixture was cooled in an ice bath and a solution of ethyl 4-chloroacetoacetate (VIII, 102.9 g) in tetrahydrofuran (250 mL) was added dropwise over a period of 1 h. The reaction mixture was stirred at room temperature for 20 h. The reaction mixture was then quenched with water (100 mL) and tetrahydrofuran was removed under reduced pressure. The aqueous phase was extracted with ethyl acetate (3×250 mL). The combined organic fractions was dried (sodium sulfate), filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (grade 9385, Merck, 230-400 mesh, 60 Å) using a mixture of hexane and ethyl acetate (9:1 and 8:2; 2L each) as eluent, thereby affording the title compound (XVI, 81.6 g). IR (neat, cm-1): 1736. (Alker, D. J. Med. Chem. 1991, 34, 19).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723618uspto-grants-1998_03