Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22262241 | HCID 22262241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22261640 | HCID 22261640 | 74.4% |
Reaction Steps
To a solution of (4RS,5SR)-5-(3-chlorophenyl)-4-[(3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl)methyl]-1,3-oxazolidin-2-one (5.33 g, 14.9 mmol) in ethanol (100 ml) was added 8N aqueous sodium hydroxide solution (9.3 ml, 74.5 mmol), and the mixture was heated under reflux for 5 hrs. After completion of the reaction, ethanol was evaporated under reduced pressure. The residue was diluted with water, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by recrystallization (hexane-ethyl acetate) to give (1RS,2SR)-2-amino-1-(3-chlorophenyl)-3-(3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-1-propanol (3.68 g, 74%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982348B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-9aa96b2728b64f158330478931c77524 |
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| Source note | uspto-grants-2006_01 |
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