Reaktion #799989

ord-7a517cee9eb1492993b2cef8096136c8

Reaktionsgleichung

CC(C)(C)OC(=O)N1C2CC2C[C@@H]1CO
(3R)-tert-butyl 3-(hydroxymethyl)-2-azabicyclo[3.1.0]hexane-2-carboxylate
CC#N.ClC(Cl)(Cl)Cl.O
MeCN CCl4 H2O
[Na+].[O-][I+3]([O-])([O-])[O-]
sodium periodate
CC(C)(C)OC(=O)N1C(C(=O)O)CC2CC21
title compound
Ausbeute 46.1%
CC(C)(C)OC(=O)N1C(C(=O)O)CC2CC21
2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid
Ausbeute 46.1%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethen quenched by addition of isopropanol (6 ml)
  2. 2
    workup.ADDITIONThe resulting black mixture was diluted with Et2O (50 ml)
  3. 3
    Filtrationfiltered through a celite pad
  4. 4
    SonstigeThe filtrate was evaporated
  5. 5
    workup.DISSOLUTIONthe residue was dissolved in water
  6. 6
    Waschenthe aqueous was washed with Et2O (3×30 ml)
  7. 7
    Extraktionre-extracted with EtOAc (3×30 ml)
  8. 8
    SonstigeCollected organics after solvent evaporation

Vorschrift

To a solution of (3R)-tert-butyl 3-(hydroxymethyl)-2-azabicyclo[3.1.0]hexane-2-carboxylate (D32) (440 mg, 2.06 mmol) in a mixture MeCN/CCl4/H2O (6/6/9 ml), sodium periodate (1.76 g, 8.25 mmol) was added and the reaction stirred vigorously for 5 min before addition of Ruthenium trichloride (12.8 mg, 0.062 mmol). The resulting solution was stirred 18 hrs at RT then quenched by addition of isopropanol (6 ml). The resulting black mixture was diluted with Et2O (50 ml) and filtered through a celite pad. The filtrate was evaporated and the residue was dissolved in water, the pH was adjusted to pH˜9-10 with K2CO3 and the aqueous was washed with Et2O (3×30 ml). Aqueous was then acidified to pH˜4-5 and re-extracted with EtOAc (3×30 ml). Collected organics after solvent evaporation afforded the title compound (D33) (216 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09181279B2uspto-grants-2015_11