Reaktion #41184

ord-25c3b70965af461399f9fca20de6164c

Reaktionsgleichung

CC(C)(C)OC(=O)NN
hydrazinecarboxylic acid tert-butyl ester
Cc1ccccc1
toluene
[K+].[OH-]
potassium hydroxide
COCCCBr
1-bromo-3-methoxypropane
COCCCN(N=C(C)C)C(=O)OC(C)(C)C
N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester
Ausbeute 98.0%

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe solution was then heated to 80° C. for 3 h
  2. 2
    TemperaturThe solution was cooled to room temperature
  3. 3
    Waschenwashed with water (3×150 mL) until the water layer
  4. 4
    TrocknenThe organic layer was dried over anhydrous magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated in vacuo

Vorschrift

To a solution of hydrazinecarboxylic acid tert-butyl ester (4.67 g, 27.16 mmol) in toluene (90 mL) was added pulverized potassium hydroxide (1.98 g, 35.3 mmol) and tetrabutylammonium hydrogensulfate (904 mg, 2.72 mmol). The solution was heated to 50° C. in a preheated oil bath and 1-bromo-3-methoxypropane (3.67 mL, 32.6 mmol) was added drop-wise over 45 minutes. The solution was then heated to 80° C. for 3 h. The solution was cooled to room temperature and washed with water (3×150 mL) until the water layer was neutral. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to provide N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester as a viscous oil (6.49 g, 98%), which was used without further purification. Mass spectrum: m/z: 245.4 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728029B2uspto-grants-2010_06