Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | (2,4-Difluorophenyl)[1-(phenylmethyl)-3-pyrrolidinyl]methanone oxime | HCID 73856697 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21960044 | HCID 21960044 | 74.8% |
Reaction Steps
A mixture of (2,4difluorophenyl)[1-(phenylmethyl)-3-pyrrolidinyl]methanone oxime (10.8 g, 34.2 mmol), potassium hydroxide (10 g), water (100 ml), and ethanol (100 ml) was heated at reflux for 2 hours. At the end of the reaction, the solution was cooled and ethanol was removed on a rotary evaporator. The aqueous mixture was diluted with water (100 ml) then extracted with dichloromethane (500 ml). The organic solution was washed with brine and dried over anhydrous MgSO4. The solution was concentrated to an oil (9.8 g). The crude product was purified by flash chromatography over a silica gel column. The product thus obtained weighed 4.46 g (44%) as a light yellow oil. The oily product was dissolved in ethanol, and then treated with a solution of fumaric acid (1.73 g, 1.0 eq) in ethanol. Crystallization took place slowly with the addition of isopropyl ether. Recrystallization from ethanol (15 ml) gave 4.6 g of 6-fluoro-3-[1-(phenylmethyl)-3-pyrrolidinyl]-1,2-benzisoxazole fumarate as white crystals, m.p. 142°-144°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05843977 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-2d7ecbd5efec4c51ad15aa79578491ee |
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| Source note | uspto-grants-1998_12 |
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