Réaction #5275

Équation de réaction

4-chloro-β-nitrostyrene

ethyl (diethoxymethyl)methylphosphinate

ammonium chloride

diisopropylamine

n-butyllithium

→

ethyl 2-(4-chlorophenyl)-3-nitropropyl(diethoxymethyl)phosphinate

Solvants

tetrahydrofuran

tetrahydrofuran

tetrahydrofuran

hexane

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONis introduced
2. 2
   workup.ADDITIONis added
3. 3
   ExtractionThe aqueous layer is then extracted with 2×25 ml of diethyl ether
4. 4
   Séchagedried over magnesium sulphate
5. 5
   AutreThe solvent is then evaporated under reduced pressure
6. 6
   Autrethe crude product chromatographed on silica gel

Mode opératoire

To a solution of 1.16 g of diisopropylamine in 40 ml of tetrahydrofuran at -78° C. under an atmosphere of nitrogen are added 7.2 ml of a 1.6M solution of n-butyllithium in hexane. This solution is then stirred for a period of 10 minutes at this temperature, after which time a solution of 2.0 g of ethyl (diethoxymethyl)methylphosphinate in 20 ml of tetrahydrofuran is added. This mixture is then stirred for a period of 1 hour at -78° C. after which time a solution of 1.75 g of 4-chloro-β-nitrostyrene in 20 ml of tetrahydrofuran is introduced. This mixture is then allowed to warm to room temperature when 40 ml of a saturated ammonium chloride solution is added. The aqueous layer is then extracted with 2×25 ml of diethyl ether and the organic extracts are combined and dried over magnesium sulphate. The solvent is then evaporated under reduced pressure and the crude product chromatographed on silica gel using ethyl acetate as an eluent to give ethyl 2-(4-chlorophenyl)-3-nitropropyl(diethoxymethyl)phosphinate as a viscous oil, 31P=+42.2 and +41.8 ppm (CDCl3).

Source