Reaktion #7020

ord-23a7463ec365497a8da5e62103007ce0

Reaktionsgleichung

CC(C)(C)OC(=O)NN
Carbazic acid tert-butyl ester
COCCCC(=O)O
4-methoxybutyric acid
CCN=C=NCCCN(C)C.Cl
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt
COCCCC(=O)NNC(=O)OC(C)(C)C
N′-(4-methoxybutyryl)hydrazine carboxylic acid tert-butyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenAfter the reaction solution was concentrated under reduced pressure, ethyl acetate
  2. 2
    workup.ADDITIONwas added to the residue, which
  3. 3
    Waschenwas then washed with aqueous 1 mol/liter hydrochloric acid solution, saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride
  4. 4
    Trocknendried over anhydrous sodium sulfate
  5. 5
    SonstigeAfter the solvent was evaporated under reduced pressure

Vorschrift

Carbazic acid tert-butyl ester (9.21 g) was dissolved in pyridine (120 ml), followed by addition of 4-methoxybutyric acid (9.06 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt (20.0 g), and stirred at ambient temperature for 64 hours. After the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, which was then washed with aqueous 1 mol/liter hydrochloric acid solution, saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, N′-(4-methoxybutyryl)hydrazine carboxylic acid tert-butyl ester was obtained in yellow oil (9.30 g, 57%). The physico-chemical values are as follows.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084164B2uspto-grants-2006_08