Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 22323781 | HCID 22323781 | — |
| Catalyst | Water | HCID 962 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(1,2-Dihydroxyethyl)chroman-4-one | HCID 67171127 | 99% |
Reaction Steps
To a mixture of 7-vinylchroman-4-one (Preparation 2D, 0.801 g, 4.60 mmol) and a 50% solution of NMO in water (0.953 mL, 4.60 mmol) in THF (11 mL) at room temperature was added a 4% aqueous solution of osmium tetroxide in water (1.44 mL, 0.184 mmol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with dichloromethane (200 mL) and washed with water (40 mL). The organic layer was collected and was washed with brine (40 mL). The combined aqueous layers were extracted with dichloromethane (200 mL), and the combined organic layers were dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded 7-(1,2-dihydroxyethyl)chroman-4-one (0.950 g, 4.56 mmol, 99% yield) as a dark yellow oil. The product had an HPLC ret. time=0.587 min.−Column: Chromolith SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=209.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216972B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2a0bd4899ef741ae987f31703fc7c41c |
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| Source note | uspto-grants-2015_12 |
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