HCID 19899068, compound → HCID 19899036, compound

2.4 g (7.5 mmol) of a cis/trans mixture of methyl 3-(4-chlorophenyl)-5,6,7,8-tetrahydro-4-hydroxy-4H-cyclohept[d]isoxazole-7-carboxylate were stirred in 150 ml of acetone and Jones' reagent was added dropwise until the orange color persisted for 20 minutes. The mixture was filtered and the residue was washed with acetone. The combined filtrate and washings were treated with isopropanol and the mixture was neutralized by stirring with solid sodium bicarbonate. The mixture was filtered. The filtrate was evaporated and the residue was partitioned between dichloromethane and water. The organic phase was dried over magnesium sulfate and evaporated. The residue was treated with hexane and the resulting solid was collected and dried to give 1.85 g of methyl 3-(4-chlorophenyl)-5,6,7,8-tetrahydro-4-oxo-4H-cyclohept[d]isoxazole-7-carboxylate of melting point 108°-109° C.

1. filtrationThe mixture was filtered
2. washthe residue was washed with acetone
3. additionThe combined filtrate and washings were treated with isopropanol
4. filtrationThe mixture was filtered
5. customThe filtrate was evaporated
6. customthe residue was partitioned between dichloromethane and water
7. dry with materialThe organic phase was dried over magnesium sulfate
8. customevaporated
9. additionThe residue was treated with hexane
10. customthe resulting solid was collected
11. customdried

ORD record

ord-69af57881a334c4399182be8efda1d31

Source dataset

uspto-grants-1992_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05114960