Reaktion #170233

ord-9525a9c43ae545a2be36e857be7c1265

Reaktionsgleichung

CC1(C)OC(=O)CC(=O)O1
Meldrum's acid
C(=NC1CCCCC1)=NC1CCCCC1
DCC
CC(C)(C)OC(=O)N1CC(C(=O)O)C1
azetidine-1,3-dicarboxylic acid mono-tert-butyl ester
C1CCCCC1
cyclohexane
CC(C)(C)OC(=O)N1CC(C(=O)C2C(=O)OC(C)(C)OC2=O)C1
title compound
CC(C)(C)OC(=O)N1CC(C(=O)C2C(=O)OC(C)(C)OC2=O)C1
3-(2,2-Dimethyl-4,6-dioxo-[1,3]dioxane-5-carbonyl)-azetidine-1-carboxylic acid tert-butyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe precipitate of dicyclohexyl urea was then filtered
  2. 2
    Waschenrinsed with diethyl ether (100 mL)
  3. 3
    workup.ADDITIONThe mother liquors were diluted with DCM (100 mL)
  4. 4
    Waschenwashed with a 1M solution of aqueous HCl (2×30 mL)
  5. 5
    Trocknendried over sodium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated to dryness

Vorschrift

Meldrum's acid (0.85 g, 5.97 mmol), DCC (1.22 g, 5.97 mmol), and DMAP (1.45 g, 11.94 mmol) were successively added to a solution of azetidine-1,3-dicarboxylic acid mono-tert-butyl ester (1.2 g, 5.97 mmol) in dichloromethane (25 mL) at room temperature. The reaction mixture was stirred overnight and then diluted by addition of cyclohexane (25 mL). The precipitate of dicyclohexyl urea was then filtered and rinsed with diethyl ether (100 mL). The mother liquors were diluted with DCM (100 mL) and washed with a 1M solution of aqueous HCl (2×30 mL), dried over sodium sulfate, filtered and concentrated to dryness. After trituration in diethyl ether the title compound was obtained as a white solid (1.9 g, 100%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846711B2uspto-grants-2014_09