Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 18429363 | HCID 18429363 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18429230 | HCID 18429230 | — |
Reaction Steps
5-[N′-(2-Propenyl)-2,3 -diacetoxypropionylamino]-3-acetoxymethyl-N-(2-acetoxyethyl)-2,4,6-triiodobenzamide (8.73 g, 9.90 mmol) was dissolved in acetone (360 ml) and water (40 ml) and the solution was cooled in an ice-bath. Osmium tetroxide (110 mg, 0.43 mmol), and an excess of t-butylhydroperoxide was added. 4-Methyl-morpholine N-oxide (2,32 g, 19.8 mmol) was added and the mixture was stirred at room temperature for 24 h. The reaction was then quenched by addition of a saturated solution of sodium hydrogen sulphite (120 ml). The acetone was evaporated, and the residue was extracted with ethyl acetate (2×70 ml). The organic extracts were washed with water (50 ml), dried (Na2SO4), and the solvent was evaporated. The residue was chromatographed on a column of silica using a mixture of ethyl acetate/acetone (1/1) as the eluent.Yield: 5.82 g (64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310243B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-93dbe4c049da472da354d5583fb95d88 |
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| Source note | uspto-grants-2001_10 |
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