Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542698Erstellt: 25. Oktober 2026

4-(4,5-Dihydro-4,4-dimethyl-2-oxazolyl)-cyclohexanone → HCID 178444407, Verbindung

https://huagongshe.com/reaction/542698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(4,5-Dihydro-4,4-dimethyl-2-oxazolyl)-cyclohexanoneHCID 13548370—
EduktHCID 178444392HCID 178444392—
EduktHCID 178444488HCID 178444488—
LösungsmittelBenzeneHCID 241—
ProduktHCID 178444407HCID 178444407—

Reaktionsschritte

1-(p-Bromophenyl)-2-(trans-4-n-pentylcyclohexyl)-ethane [obtainable by Friedel-Crafts acylation of benzene with trans-4-n-pentylcyclohexylacetyl chloride, Wolff-Kishner reduction of the carbonyl group and bromination of the aromatic in the p-position] is subjected to a Grignard reaction with 4-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-cyclohexanone. Detachment of water, with simultaneous removal of the oxazolyl protective group, by boiling with ethanolic H2SO4, hydrogenation of the double bond, conversion of the ethyl ester into the amide, dehydration analogously to Example 2 and customary working up gives 1-[p-(trans-4-cyanocyclohexyl)-phenyl]-2-(trans-4-n-pentylcyclohexyl)-ethane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04659502
Quelldatensatzuspto-grants-1987_04
ORD IDord-d8550308f1de45729c13a65157713ce5
Quellennotizuspto-grants-1987_04