HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Bromoquinoline → 3-(Dimethoxyacetyl)quinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Bromoquinoline | HCID 21413 | — |
| Edukt | N-(dimethoxyacetyl)morpholine | HCID 21298597 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(Dimethoxyacetyl)quinoline | HCID 14276934 | — |
Reaktionsschritte
3-Bromoquinoline (3.29 ml., 0.032 mol) was dissolved in 300 ml. THF and cooled to -78°. n-Butyllithium (13.6 ml. of 2.5M in hexane, 0.034 ml.) was added slowly and the mixture stirred 15 minutes at -75° to -78°. N-(Dimethoxyacetyl)morpholine (5.98 g., 0.032 mol) in 10 ml. THF was then added and stirring continued for 1.75 hours at the same temperature. The reaction was then quenched into 300 ml. saturated NH4Cl. The aqueous layer was separated and extracted 4×100 ml. ether. The organic layers were combined, dried over MgSO4, stripped to yield title product, 7.0 g., bp 120°-123°/0.125 torr.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04762921 |
| Quelldatensatz | uspto-grants-1988_08 |
| ORD ID | ord-97c01dee82af4b81ba08bf372d90172a |
| Quellennotiz | uspto-grants-1988_08 |