HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Toluene → 4'-((2-Butyl-4-oxo-1,3-diazaspiro(4.4)non-1-ene-3-yl)methyl)(1,1'-biphenyl)-2-carbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4'-(Bromomethyl)-2-cyanobiphenyl | HCID 1501912 | — |
| Edukt | 2-Butyl-1,3-diazaspiro[4.4]nonan-4-one hydrochloride | HCID 22117883 | — |
| Katalysator | Tributylmethylammonium chloride | HCID 91822 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4'-((2-Butyl-4-oxo-1,3-diazaspiro(4.4)non-1-ene-3-yl)methyl)(1,1'-biphenyl)-2-carbonitrile | HCID 9843116 | 85,7% |
Reaktionsschritte
A mixture of 0.231 g (1.0 mmol) of 2-butyl-1,3-diazaspiro [4.4]nonan-4-one, hydrochloride, 0.272 g (1.0 mmol) of 4'-(bromomethyl)[1,1'-biphenyl]-2-carbonitrile, 24.4 μL (0.075 mmol) of 75% aqueous solution of methyl-tributylammonium chloride, 2.0 mL of toluene and 2.0 mL of 50% aqueous solution of sodium hydroxide was vigorously stirred at room temperature for 2.2 hours. Then the reaction mixture was diluted with 2 mL of water and the two phases separated. The organic phase was extracted twice with 2 mL of water, evaporated under vacuum to give 0.33 g (85.7%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06162922 |
| Quelldatensatz | uspto-grants-2000_12 |
| ORD ID | ord-5e5224e00cd642edb0050072f3bdc298 |
| Quellennotiz | uspto-grants-2000_12 |