Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | HCID 68450766 | HCID 68450766 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 136335802 | HCID 136335802 | 30.2% |
Reaction Steps
Boron trichloride solution (2 ml, 11.0M in dichloromethane) was added slowly to a solution of 3-{2,4-Bis-benzyloxy-5-[4-(4-methoxy-phenyl)-3-methyl-isoxazol-5-yl]-phenyl}acrylic acid tert-butyl ester (50 mg, 0.09 mmol) in dichloromethane (1 ml), at −78° C. (dry ice/acetone) under a nitrogen atmosphere. The resulting solution was stirred for ˜1 hr at −78° C., and for ˜90 mins. at room temperature. The solution was cooled to −78° C. and water (2 ml) added and the mixture was stirred for ˜30 mins at room temperature. Ethyl acetate (30 ml) was added and the solution washed with water (2×5 ml) and saturated aqueous sodium chloride solution (10 ml). The solution was dried over anhydrous magnesium sulphate and concentrated to a pale yellow gum. Trituration with hexane gave a yellow solid, solids were removed by filtration and washed with hexane, dried in vacuo, to give 3-{2,4-dihydroxy-5-[4-(4-methoxy-phenyl)-3-methyl-isoxazol-5-yl]-phenyl}-acrylic acid (10 mg) as yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705027B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-66a0f51de0da42c68d826309dfa65c79 |
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| Source note | uspto-grants-2010_04 |
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