Acetone → Nonyl isocyanate

HRID 641078Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 641078
C(Cl)(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[N-]=[N+]=[N-].[Na+].[N-:17]=[N+]=[N-].C1(C)C=CC=CC=1.C[C:28](C)=[O:29]>O>[CH2:2]([N:17]=[C:28]=[O:29])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Komponenten

7

Edukt 5

HCID 180AcetoneHCID 1140TolueneHCID 33557Sodium AzideHCID 33558AzideHCID 66982Decanoyl chloride

Produkt 1

HCID 11275250Nonyl isocyanateAusbeute 47 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

A solution of decanoyl chloride (20 g, 104.8 mmoles) in acetone (30 ml) was dropped into a solution of sodium azide (9.53 g, 146.6 mmoles) in water (30 ml), cooled in an ice bath. The temperature of the azide solution was kept between 10 and 15° C. after one hour, the solution was transferred in a separatory funnel and the lower phase (the aquoeus one) was eliminated. The higher phase was transferred into a flask containing 100 ml of toluene, previously warmed at 65° C. After 1.5 hours, the solution was evaporated to dryness, giving 13.37 g crude product, which after vacuum distillation gave 8.3 g pure product in the form of colorless liquid.

Aufarbeitung

  1. temperaturecooled in an ice bath
  2. customthe solution was transferred in a separatory funnel
  3. customThe higher phase was transferred into a flask
  4. customthe solution was evaporated to dryness
  5. customgiving 13.37 g crude product, which
  6. distillationafter vacuum distillation

Quellen und Nachweise

ORD-Eintrag
ord-4af9769118b242ff82c633899ff9203c
Quelldatensatz
uspto-grants-2010_04
Patentnummer
USRE041226E1

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