Reaktion #2362432

ord-6c6aaf4f114d4f1bb4de7135a8a82b90

Reaktionsgleichung

CC(C)(C)C(C(=O)O)C(=O)O
Mono-tert-butyl malonic acid
[Cl-].[Cl-].[Mg+2]
magnesium chloride
O=C(n1ccnc1)n1ccnc1
CDI
CCc1ccc(C(C)(C)C(=O)O)cc1I
2-(4-ethyl-3-iodophenyl)-2-methylpropanoic acid
CCc1ccc(C(C)(C)C(=O)C(C(=O)O)C(C)(C)C)cc1I
title compound
CCc1ccc(C(C)(C)C(=O)C(C(=O)O)C(C)(C)C)cc1I
Tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred at room temperature for 1 hr
  2. 2
    Sonstigeto prepare a solution
  3. 3
    workup.ADDITIONThis solution was then added dropwise to the aforementioned mixture
  4. 4
    Waschenthe resulting solution was washed with DME (90 ml)
  5. 5
    workup.STIRRINGstirred at 70° C. for 3 hrs
  6. 6
    workup.ADDITIONThe reaction mixture was diluted with isopropyl acetate (225 ml) and heptane (225 ml)
  7. 7
    Waschenthe organic layer was washed with 2 N hydrochloric acid (684 ml), 0.17 N hydrochloric acid (540 ml), 15% aqueous solution of ammonium chloride (540 ml), 1 N aqueous solution of sodium hydroxide (540 ml) and 15% brine (540 ml) in order
  8. 8
    EinengenThe organic layer was concentrated under reduced pressure

Vorschrift

Mono-tert-butyl malonic acid (72.5 g) was dissolved in DME (360 ml), added with TEA (189 ml) and magnesium chloride (29.63 g) and the mixture was stirred for 2 hrs. In a separate vessel, CDI (52.75 g) was added to the DME (360 ml) solution of 2-(4-ethyl-3-iodophenyl)-2-methylpropanoic acid (90 g) and stirred at room temperature for 1 hr to prepare a solution. This solution was then added dropwise to the aforementioned mixture, and the resulting solution was washed with DME (90 ml) and stirred at 70° C. for 3 hrs. The reaction mixture was diluted with isopropyl acetate (225 ml) and heptane (225 ml), and the organic layer was washed with 2 N hydrochloric acid (684 ml), 0.17 N hydrochloric acid (540 ml), 15% aqueous solution of ammonium chloride (540 ml), 1 N aqueous solution of sodium hydroxide (540 ml) and 15% brine (540 ml) in order. The organic layer was concentrated under reduced pressure to obtain the title compound as a crude product, which was used for the next step without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09126931B2uspto-grants-2015_09