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Sodium Cyanide → Sodium Cyanide

HRID 67880
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Reaktionsgleichung

Reaktionsgleichung von HRID 67880
[NH3:1].[C:2]1([CH3:23])[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[B:8]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH3:15].[C-:24]#N.[Na+:26]>O.[OH-].[NH4+].O.O.O.O.O.O.[Ni](Cl)Cl>[C-:24]#[N:1].[Na+:26].[C:2]1([CH3:23])[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[B:8]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH3:15]
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Komponenten

7

Edukt 2

HCID 8929Sodium CyanideHCID 20526448Tri-o-tolylborane ammonia

Produkt 2

HCID 8929Sodium CyanideHCID 12430998Tris(2-methylphenyl)borane

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 11791229Dichloronickel;hexahydrateKatalysatorHCID 962Water
Lösungsmittel
HCID 14923Ammonium HydroxideLösungsmittel2×

Versuchsvorschrift

A sodium cyanide adduct of tri-o-tolylborane was prepared by dissolving 2.1731 g of the tri-o-tolylborane ammonia adduct [(o-CH3C6H4)3BNH3 ] and 0.3495 g of sodium cyanide in 100 ml of distilled water, following which approximately 80 ml of ammonium hydroxide was distilled from the solution at atmospheric pressure. An additional 100 ml of distilled water was then added to the distillation flask and 100 ml of dilute ammonium hydroxide distilled therefrom. This resultant solution was then combined at room temperature under agitation with a solution prepared by dissolving 0.8608 g of nickel chloride hexahydrate in 50 ml of concentrated ammonium hydroxide (28-30% NH3). The gray precipitate which formed as the solutions were combined was collected by vacuum filtration, washed with 100 ml of concentrated ammonium hydroxide and then dried under vacuum at 50° C. for 4 hours. The product which weighed 2.4069 g was submitted for elemental analysis. The results of the analysis and the calculated formula for the complex Ni[NH3 ]4 [(NC)B(C6H4CH3 -o)3 ]2 are set forth below.

Aufarbeitung

  1. distillationwas distilled from the solution at atmospheric pressure
  2. additionAn additional 100 ml of distilled water was then added to the distillation flask and 100 ml of dilute ammonium hydroxide
  3. distillationdistilled
  4. customwas then combined at room temperature under agitation with a solution
  5. customprepared
  6. customThe gray precipitate which formed as the solutions
  7. filtrationwere combined was collected by vacuum filtration
  8. washwashed with 100 ml of concentrated ammonium hydroxide
  9. customdried under vacuum at 50° C. for 4 hours
  10. customThe results of the analysis

Quellen und Nachweise

ORD-Eintrag
ord-65599b480f224c92bde4e20f790dccd9
Quelldatensatz
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04347193

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