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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048999Generated: November 4, 2026

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

https://huagongshe.com/reaction/2048999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantCarbonate IonHCID 19660—
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 potassim 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 numberUS04196120
Source datasetuspto-grants-1980_04
ORD IDord-5e9daad682a24c16a649a652f5ae6cf0
Source noteuspto-grants-1980_04