Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 118071495 | HCID 118071495 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Methyl morpholine oxide | HCID 82029 | — |
| Product | HCID 118071468 | HCID 118071468 | — |
Reaction Steps
To a mixture of 2-allyl-6-chloro-4-nitrophenol (30.0 g), acetone (270 mL), and water (30.0 mL) were added a 2.5 wt % osmium (VIII) oxide solution in tert-butanol (10.0 mL) and 4-methylmorpholin-4-oxide (18.1 g), followed by stirring at room temperature for 41 hours. The reaction mixture was concentrated under reduced pressure, acidified with 1 M hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. The insoluble materials were separated by filtration, the filtrate was concentrated under reduced pressure, and the obtained solid was washed with a mixed solvent of chloroform and hexane to obtain 3-(3-chloro-2-hydroxy-5-nitrophenyl)propane-1,2-diol (20.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260445B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-8cdd44dac73b43968aa54dd40c852bea |
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| Source note | uspto-grants-2016_02 |
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