HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dibenamine hydrochloride → alpha-(N,N-dibenzylaminoethyl) benzyl cyanide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dibenamine hydrochloride | HCID 5925 | — |
| Edukt | Phenylacetonitrile | HCID 8794 | — |
| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | alpha-(N,N-dibenzylaminoethyl) benzyl cyanide | HCID 54062416 | 94% |
Reaktionsbedingungen
| Temperatur | 50 °C |
|---|
Reaktionsschritte
Benzyl cyanide (0.97 mL, 8.4 mmole) was reacted with lithium bis(trimethylsilyl)amide (LHMDSA) (8.4 mL, 8.4 mmole) in 5 mL of THF at -78° C. for 1 hour. After an additional aliquot of LHMDSA (4.2 mL, 4.2 mmole) was added, N-(2-chloroethyl)dibenzylamine hydrochloride (1.0 g, 3.4 mmole) was then added. The reaction was allowed to stand at room temperature and was then warmed to 50° C. for 3.5 hours. The mixture was poured into ice/water, and the product was extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure to afford alpha-(N,N-dibenzylaminoethyl) benzyl cyanide (1.05 g), isolated in 94% yield (MS: (M+H)+ =341).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05190922 |
| Quelldatensatz | uspto-grants-1993_03 |
| ORD ID | ord-c8eeb9d2ead14d3bbc0fb1dc636b3199 |
| Quellennotiz | uspto-grants-1993_03 |