Water → 5-(3-Chlorophenyl)-6,7-dihydro-3-(3-fluorophenyl)-1,2-benzisoxazol-4(5H)-one

Temperature

-78 °C

In a similar manner to that of Examples 7a-d starting with 3-fluorobenzaldehyde oxime, the starting ketone is prepared. In 200 ml anhydrous THF was dissolved 11.4 g 6,7-dihydro-3-(3-fluorophenyl)-1,2-benziaoxazol-4(5H)-one under nitrogen atmosphere with stirring. The solution was cooled to -78° C. and 49.4 ml lithium diisopropylamide (1.5 molar in cyclohexane) was added dropwise. The resulting solution was stirred for ten minutes at -78° C. and 6.4 ml 1-chloro-3-iodopropane was added. Upon warming to room temperature, the reaction mixture was poured into water and ether. The layers were separated and the aqueous phase was extracted twice with dichloromethane and once with ether. The combined organic layers were washed with brine and dried (MgSO4). Filtration and concentration gave the crude product. Column chromatography on silica gel (start with 10% dichloromethane in hexane and gradually increase polarity to 100% dichloromethane) gave 4.5 g of 5-(3-chloropropyl)-6,7-dihydro-3-(3-fluorophenyl)-1,2 -benzisoxazol-4(5H)-one.

1. stirringThe resulting solution was stirred for ten minutes at -78° C.
2. temperatureUpon warming to room temperature
3. customThe layers were separated
4. extractionthe aqueous phase was extracted twice with dichloromethane and once with ether
5. washThe combined organic layers were washed with brine
6. dry with materialdried (MgSO4)
7. filtrationFiltration and concentration
8. customgave the crude product

ORD record

ord-1e4f90c92c604ee8b2386fe218d63658

Source dataset

uspto-grants-1993_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05180834