Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 13537592 | HCID 13537592 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13537598 | HCID 13537598 | — |
Reaction Steps
To a mixture of 13.5 g of 2-[3-(4-fluorobenzoyl)-isoxazol-5-yl]ethanol and a few crystals of tetrabutylammonium hydrogen sulfate in 1 liter of CH2Cl2 was added 150 ml of 9M H2SO4. To this was added 16.9 g of pulverized K2Cr2O7 and the mixture was stirred at room temperature for 1 hour. The organic phase was separated from the aqueous phase and washed with water. The acid product was extracted from the organic phase using 100 ml of 5% NaHCO3. The alkaline solution was washed with CH2Cl2 several times, until all of the neutral impurities were removed, and then acidified slowly with 5% HCl. The precipitated solid was collected, washed with water and dried to yield 6.7 g of a powder. Recrystallization from 180 ml of 50% toluene/hexane gave 5.9 g (41%) of crystals, m.p. 113°-115°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04562187 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-71c14408547640d489a7c87cb6a0497f |
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| Source note | uspto-grants-1985_12 |
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