Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 23323871 | HCID 23323871 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13832256 | HCID 13832256 | — |
Reaction Steps
4-(4-Chlorophenyl)-5-(3-hydroxypropyl)-3-methylenetetrahydro-2-furanone (100 mg) was dissolved in acetone (2 ml), and Jones reagent (0.25 ml) was added dropwise with ice-cooling. The mixture was stirred at the same temperature for 2 hours, poured into ice water (20 ml) and extracted with ethyl acetate. The extract was washed with water and dried over magnesium sulfate. The solvent was then distilled off to give crude 3-[3-(4-chlorophenyl)-5-oxo-4-methylenetetrahydro-2-furyl]propionic acid (80 mg) as an oil. The above compound was dissolved in dioxane (5 ml)-water (2 ml), and osmic acid (10 mg) was added. The mixture was stirred at room temperature for 5 minutes. To the reaction mixture was added portionwise sodium periodate (500 mg), and the mixture was stirred at the same temperature for 4 hours, followed by addition of water (20 ml) and extraction with ethyl acetate. The extract was washed with water and dried over magnesium sulfate. The solvent was then distilled off and the residue was purified by preparative silica gel thin layer chromatography (developer: 10% methanol-chloroform) to give 3-[3-(4-chlorophenyl)-4-hydroxy-5-oxo-2,5-dihydro-2-furyl]propionic acid (20 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04585789 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-395b2356b9e74e9585d46cfcf4df509e |
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| Source note | uspto-grants-1986_04 |
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