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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66292Generated: November 1, 2026

Iodoethane → 3-Formyl-1-(p-ethoxyphenyl)-3-azabicyclo[3.1.0]hexane

https://huagongshe.com/reaction/66292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexaneHCID 12719876—
SolventEthanolHCID 702—
Product3-Formyl-1-(p-ethoxyphenyl)-3-azabicyclo[3.1.0]hexaneHCID 1271988227.2%

Reaction Steps

To a stirred mixture of 1.0 g of 3-formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane and 0.7 g of potassium carbonate in 25 ml of absolute ethanol is added a solution of 3.2 g of ethyl iodide in 10 ml of absolute ethanol. The mixture is refluxed for 2 hours and then is filtered and evaporated. The residual mixture of crystals and liquid is combined with water and this is extracted with chloroform and the extract is dried over magnesium sulfate and evaporated to give 1.0 g of a colorless, viscous liquid, which crystallizes on standing. Recrystallization from hexane gives 0.31 g of 3-formyl-1-(p-ethoxyphenyl)-3-azabicyclo[3.1.0]hexane as colorless crystals, m.p. 48°-51° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04131611
Source datasetuspto-grants-1978_12
ORD IDord-1721ece03c8d45d890242264ded299fc
Source noteuspto-grants-1978_12