Réaction #55573

Équation de réaction

1-(3-ethylcyclobutyl)-trans-3-iodoprop-2-en-1-ol

ethylvinyl ether

→

title compound

Rendement 69.0%

1-iodo-3-(1-ethoxyethoxy)-3-(3-ethylcyclobutyl)-1E-propene

Rendement 69.0%

Solvants

sodium bicarbonate

Conditions de réaction

Traitement

1. 1
   Autrewas prepared
2. 2
   Extractionthe products were extracted with 150 ml (3×50 ml) of ether
3. 3
   ExtractionThe combined ether extract
4. 4
   Lavagewas washed with 50 ml of saturated aqueous sodium chloride
5. 5
   Séchagedried over anhydrous magnesium sulfate
6. 6
   Filtrationfiltered
7. 7
   Autrethe solvent was removed in vacuo
8. 8
   AutreThe residue was chromatographed on silica gel 60 (0.063-0.2 mm, 70-230 mesh, ASTM)

Mode opératoire

A mixture containing 4.8 g (0.018 mole) of 1-(3-ethylcyclobutyl)-trans-3-iodoprop-2-en-1-ol (prepared in 1I) and 38.2 g (50 ml, 0.51 mole) of ethylvinyl ether (Aldrich Chemical Company; Beilstein 1:433) was prepared. One drop of phosphorus oxychloride was added thereto and the mixture was allowed to stir for about 15 hr at room temperature. The mixture was poured into 50 ml of saturated aqueous sodium bicarbonate and the products were extracted with 150 ml (3×50 ml) of ether. The combined ether extract was washed with 50 ml of saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and the solvent was removed in vacuo. The residue was chromatographed on silica gel 60 (0.063-0.2 mm, 70-230 mesh, ASTM) using chloroform as the eluant to yield 4.2 g of the title compound having the following physical characteristics:

Source