Reacción #4509
ord-af833aac68e84efd9b9b7fe09d4bd9be
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Filtraciónthe precipitate filtered off
- 2Otrosolvent removed from the filtrate under reduced pressure
- 3workup.DISSOLUTIONThe residue was dissolved in 5 ml of tetrahydrofuran and to this solution
- 4workup.ADDITIONwas added dropwise a solution of ammonia in tetrahydrofuran until the reaction
- 5workup.ADDITIONThe mixture was poured into water
- 6Extracciónextracted with ethyl acetate
- 7SecadoThe organic solution was dried over magnesium sulfate
- 8Otroevaporated to an oil which
- 9Otrowas chromatographed on silica gel
- 10Lavadoeluting with a 1:1 mixture of ethyl acetate and hexane
- 11workup.STIRRINGThe purified product was stirred with a mixture of ether and hexane
- 12Filtraciónfiltered
Procedimiento
To a solution of 500 mgs of ethyl (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-thiohexenoate in 10 ml of benzene cooled in an ice bath was added 0.1 ml of pyridine and 6 ml of a 12.5% solution of phosgene in benzene. The solution was stirred at 25° C. overnight, the precipitate filtered off and solvent removed from the filtrate under reduced pressure. The residue was dissolved in 5 ml of tetrahydrofuran and to this solution was added dropwise a solution of ammonia in tetrahydrofuran until the reaction was complete. The mixture was poured into water and extracted with ethyl acetate. The organic solution was dried over magnesium sulfate and evaporated to an oil which was chromatographed on silica gel, eluting with a 1:1 mixture of ethyl acetate and hexane. The purified product was stirred with a mixture of ether and hexane and filtered giving ethyl (E)-6-(1,3-dihydro-4-carbamoyl oxy-6-methoxy-7-methyl-3-oxo-5-iso benzofuranyl)-4-methyl-4-thiohexenoate, mp 145°-147° C.