HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 3-Formyl-1-(p-ethoxyphenyl)-3-azabicyclo[3.1.0]hexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane | HCID 12719876 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Formyl-1-(p-ethoxyphenyl)-3-azabicyclo[3.1.0]hexane | HCID 12719882 | 27.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04231935 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-23ae7b409e2c4e6d8be34f741f10ee6a |
| Source note | uspto-grants-1980_11 |