Reaktion #2032038

ord-f9ec506eb84e4d2bad606baedbe4d8f7

Reaktionsgleichung

O=S(=O)([O-])[O-].[Mg+2]
MgSO4
CC(C)(C)OC(=O)NCCCCCCO
Intermediate 20
CC(C)(C)OC(=O)NCCCCCCO
tert-Butyl (6-hydroxyhexyl)carbamate
[Na+].[OH-]
NaOH
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LAH
CNCCCCCCO
title compound
CNCCCCCCO
6-(Methylamino)hexan-1-ol

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux for 3 h
  2. 2
    TemperaturAfter 3 h the reaction was cooled to 0° C.
  3. 3
    workup.STIRRINGstirred for another 30 min
  4. 4
    FiltrationThe mixture was filtered through celite
  5. 5
    Waschenwashed with THF
  6. 6
    Einengenconcentrated

Vorschrift

Intermediate 20 (2.14 mmol) was added to a stirring solution at 0° C. containing 95% LAH (0.426 g, 10.68 mmol) in 10 mL of anhydrous THF. This mixture was then heated to 80° C. and allowed to reflux for 3 h. After 3 h the reaction was cooled to 0° C. and water (0.426 mL), 20% (w/v) NaOH (0.426 mL), and water (1.215 mL) were added sequentially. This was stirred for 15 min at rt then MgSO4 was added and stirred for another 30 min. The mixture was filtered through celite, washed with THF, and concentrated to give the title compound. The compound was used with no further purification. ES/MS calcd. for C7H18NO+ 132.1. Found m/z=132 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08394829B2uspto-grants-2013_03