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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071861Generated: October 27, 2026

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

https://huagongshe.com/reaction/2071861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-t-Butylazo-1-chlorocyclohexaneHCID 23344784—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
Product1-t-Butylazo-1-phenylcyclohexaneHCID 20288890—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a clean, dry 250 ml. round bottom 4 neck flask equipped with a magnetic stirrer, thermometer, condenser and addition funnel, which was being purged with nitrogen, was added an ether solution containing 0.06 moles of phenyl-magnesium bromide. The solution was cooled to 5° C. and a solution of 8.7 g. (0.043 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, dried 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04048423
Source datasetuspto-grants-1977_09
ORD IDord-bb075f2eb8c64ea98d2e6eedf9b9aa63
Source noteuspto-grants-1977_09