Dimethyl Sulfoxide → 1-(Azidomethyl)-3,5-bis(trifluoromethyl)benzene

HRID 1620796

Reaktionsgleichung

Reaktionsgleichung von HRID 1620796
[N-:1]=[N+:2]=[N-:3].[Na+].CS(C)=O.[F:9][C:10]([F:24])([F:23])[C:11]1[CH:12]=[C:13]([CH:16]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:18]=1)[CH2:14]Cl>O>[N:1]([CH2:14][C:13]1[CH:16]=[C:17]([C:19]([F:21])([F:22])[F:20])[CH:18]=[C:11]([C:10]([F:9])([F:23])[F:24])[CH:12]=1)=[N+:2]=[N-:3]

Komponenten

5

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

Sodium azide (74.3 g, 1.14 mol) is suspended in water (125 mL), then DMSO (625 mL) is added. After stirring for 30 minutes, a solution consisting of 3,5-Bis(trifluoromethyl)benzyl chloride (255.3 g, 0.97 moles) and DMSO (500 mL) is added over 30 minutes. (The 3,5-Bis(trifluoromethyl)benzyl chloride is heated to 35° C. to liquefy prior to dispensing (MP=30-32° C.)). The benzyl chloride feed vessel is rinsed with DMSO (50 mL) into the sodium azide solution, the mixture is heated to 40° C., and then maintained for an hour at 40° C., then cooled to 23° C.

Aufarbeitung

  1. additionis added over 30 minutes
  2. washThe benzyl chloride feed vessel is rinsed with DMSO (50 mL) into the sodium azide solution
  3. temperaturemaintained for an hour at 40° C.
  4. temperaturecooled to 23° C.

Quellen und Nachweise

ORD-Eintrag
ord-ac037c254dfd47ffaab08cedc7a253c6
Quelldatensatz
uspto-grants-2014_07
Patentnummer
US08772496B2

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