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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224295Generated: October 30, 2026

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

https://huagongshe.com/reaction/224295

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 numberUS04231935
Source datasetuspto-grants-1980_11
ORD IDord-23ae7b409e2c4e6d8be34f741f10ee6a
Source noteuspto-grants-1980_11