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

Sodium Azide → trans-Ethyl 2-azidomethyl-1-cyclopropanecarboxylate

HRID 1680338
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1680338
CS(O[CH2:6][C@@H:7]1[CH2:9][C@H:8]1[C:10]([O:12][CH2:13][CH3:14])=[O:11])(=O)=O.[N-:15]=[N+:16]=[N-:17].[Na+]>CS(C)=O>[N:15]([CH2:6][C@@H:7]1[CH2:9][C@H:8]1[C:10]([O:12][CH2:13][CH3:14])=[O:11])=[N+:16]=[N-:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 33557Sodium AzideHCID 53825740(1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylate

Produkt 1

HCID 22816282trans-Ethyl 2-azidomethyl-1-cyclopropanecarboxylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 679Dimethyl SulfoxideLösungsmittel

Versuchsvorschrift

The trans-ethyl 2-methanesulfonyloxymethyl-1-cyclopropanecarboxylate from the previous step (1.655 g, 7.45 mmol) was dissolved in dry dimethyl sulfoxide (20 ml), treated with sodium azide (0.969 g, 14.89 mmol), and stirred at room temperature for 16 h. (tlc indicated no substrate left). After dilution with water, (50 ml), the reaction mixture was extracted with ether (3×50 ml) and the combined organic extracts washed several times (×6) with water and then brine (×3). After drying on anhydrous magnesium sulfate, evaporation of the solvent under reduced pessure gave an oil. Bulb to bulb distillation gave a clear liquid; 1.178 g (93%); bp 86°-90° C./4.0 mm Hg (air bath temperature); ir (film) νmax : 2090 (N3), 1725 cm-1 (C=0); -1Hmr (CDCl3) δ: 4.13 (2H, q, J=7, CH2 --CH3), 3.21 (2H, d, J= 6, CH2 --OMs), 2.0-0.6 (4H, m, cyclopropyl), 1.23 (3H, t, 5.7 CH2 --CH3). Anal. calcd for C7H11N3O2 : C 49.69, H 6.55, N 24.83; found: C 49.81, H 6.71, N 24.29.

Aufarbeitung

  1. waitno substrate left)
  2. extractionAfter dilution with water, (50 ml), the reaction mixture was extracted with ether (3×50 ml)
  3. washthe combined organic extracts washed several times (×6) with water
  4. dry with materialAfter drying on anhydrous magnesium sulfate, evaporation of the solvent
  5. customgave an oil
  6. distillationBulb to bulb distillation
  7. customgave a clear liquid

Quellen und Nachweise

ORD-Eintrag
ord-ccc9a3d2d4894e468cdd3f4ddc8fe5c9
Quelldatensatz
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04272437

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion