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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436361Erstellt: 26. Oktober 2026

1-t-Butylazo-1-chlorocyclohexane → 1-t-Butylazo-1-phenylcyclohexane

https://huagongshe.com/reaction/436361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-t-Butylazo-1-chlorocyclohexaneHCID 23344784—
EduktHCID 178418255HCID 178418255—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-t-Butylazo-1-phenylcyclohexaneHCID 20288890—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a clean, dry 250 ml. round bottom + neck flask equipped with a magnetic stirrer, thermometer, condenser and addition funnel, which was being purged with nitrogen, was added an ether solution containing .06 moles of phenylmagnesium bromide. The solution was cooled to 5° C. and a solution of 8.7 g. (.043 moles) of 1-t-butylazo-1-chlorocyclohexane in 50 ml. of ether was added dropwise over 1/2 hour. After the addition was complete, the reaction was stirred for 15 minutes at room temperature and the excess phenylmagnesium bromide destroyed by the addition of wet ether. The reaction mixture was poured into 200 ml. of cold water and the ether layer separated, washed with 5% HCl, saturated sodium bicarbonate solution, saturated sodium chloride solution, dired over anhydrous sodium sulfate, filtered and the ether removed on a rotating evaporator leaving 9.75 g. (93%) of a yellow liquid. The infrared spectrum of the product was in agreement with the structure of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04008273
Quelldatensatzuspto-grants-1977_02
ORD IDord-5cfba88e039b4ff29c7484247454ecae
Quellennotizuspto-grants-1977_02