StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Diazomethane → Methyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetate

HRID 971703
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 971703
[N+](=[CH2:3])=[N-].[CH3:4][C:5]1[N:9]=[C:8]([CH2:10][C:11]([OH:13])=[O:12])[O:7][N:6]=1>C(OCC)C.O>[CH3:4][C:5]1[N:9]=[C:8]([CH2:10][C:11]([O:13][CH3:3])=[O:12])[O:7][N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 9550DiazomethaneHCID 213130182-(3-Methyl-1,2,4-oxadiazol-5-yl)acetic acid

Produkt 1

HCID 54453761Methyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 3283Diethyl EtherLösungsmittel2×

Versuchsvorschrift

A solution of an excess of diazomethane in diethyl ether was added to a stirred, cold (about 2° C.) solution of 14 g of 3-methyl-1,2,4-oxadiazol-5-yl-acetic acid in 500 ml of diethyl ether. After the initially vigorous evolution of nitrogen was finished, the solution was concentrated on the steam bath to about 250 ml. The solution was washed three times with 100 ml of water and the wash waters were combined, adjusted to a pH of 9.0 and were extracted with diethyl ether to obtain the part of the product which dissolved in water during the washings. The combined ethereal extracts were filtered through a water repelling paper filter and then were evaporated in vacuo. After keeping the residue for 1 hour at 8 mm the residual oil weighed 14.8 g. The yellow oil was distilled at 0.4-0.5 mm and the collected fraction with a boiling point 70°-71° C. to obtain 12.3 g of methyl 3-methyl-1,2,4-oxadiazol-5-yl-acetate with a refractive index nD25 =1.4472.

Aufarbeitung

  1. concentrationthe solution was concentrated on the steam bath to about 250 ml
  2. washThe solution was washed three times with 100 ml of water
  3. extractionwere extracted with diethyl ether
  4. customto obtain the part of the product which
  5. filtrationThe combined ethereal extracts were filtered through a water repelling paper
  6. filtrationfilter
  7. customwere evaporated in vacuo
  8. customfor 1 hour
  9. distillationThe yellow oil was distilled at 0.4-0.5 mm

Quellen und Nachweise

ORD-Eintrag
ord-fd4f19c45b1d42878442d5569fdcd58b
Quelldatensatz
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04160829

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion