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Trifluoroacetic acid → HCID 178470518, Verbindung

HRID 52606
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 52606
FC(F)(F)C(O)=O.[N-:8]=[N+:9]=[N-:10].[Na+].[C:12]([C:14]([O:16][CH2:17][CH3:18])=[O:15])#[N:13]>N1C(C)=CC=CC=1C>[CH2:17]([O:16][C:14]([C:12]1[NH:13][N:10]=[N:9][N:8]=1)=[O:15])[CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6422Trifluoroacetic acidHCID 33557Sodium AzideHCID 69336Ethyl cyanoformate

Produkt 1

HCID 178470518HCID 178470518, VerbindungAusbeute 52,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 79372,6-LutidineLösungsmittel

Versuchsvorschrift

Trifluoroacetic acid (24.47 g, 0.21M) was added dropwise over 0.5 hr under nitrogen to a stirred suspension of sodium azide (12.59 g, 0.19M) in 2,6lutidine (100 ml) at 8° to 12°. After stirring for 7 minutes ethyl cyanoformate (20.4 g, 0.20M) was added in one portion. The mixture was heated and stirred at 75° for 6 hours and then, after cooling, stirred at 20° for 16 hr. After cooling to 10° the mixture was added to ice (250 g) and 11 molar hydrochloric add (100 ml) keeping the temperature below 20°. The product was extracted into ethyl acetate (1×250, 1×200, 2×100 ml) and the combined extracts dried over magnesium sulphate. After evaporation of the solvent under reduced pressure the oily product (38.22 g) was taken up in ether (50 ml) and hexane (25 ml) added. Storage at 4° for 2-3 days produced crystalline ethyl-1H-tetrazole-5-carboxylate that was filtered off, washed with chilled ether, and air dried, 14.12 g (52.6% yield), m.p. 88°-93°.

Aufarbeitung

  1. additionwas added in one portion
  2. temperatureThe mixture was heated
  3. temperatureafter cooling
  4. stirringstirred at 20° for 16 hr
  5. temperatureAfter cooling to 10° the mixture
  6. additionhydrochloric add (100 ml)
  7. customthe temperature below 20°
  8. extractionThe product was extracted into ethyl acetate (1×250, 1×200, 2×100 ml)
  9. dry with materialthe combined extracts dried over magnesium sulphate
  10. customAfter evaporation of the solvent under reduced pressure the oily product (38.22 g)
  11. additionhexane (25 ml) added

Quellen und Nachweise

ORD-Eintrag
ord-cd980bb000e14269a008b39af27df53a
Quelldatensatz
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05616721

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