Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Oxazolidinone | HCID 73949 | — |
| Reactant | 3-Fluorophenylamine hydrochloride | HCID 2755765 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18770550 | HCID 18770550 | — |
Reaction Steps
Equimolar quantities (45.7 mmol) of 2-oxazolidinone and 3-fluoroaniline hydrochloride were combined, heated to 165° C., and stirred for 18 hours. The dark-colored mixture was allowed to cool to ambient temperature and treated with ethanol (125 mL). The suspension was heated to reflux for 1 hour, allowed to cool to ambient temperature, treated with diethyl ether (125 mL), and the suspension was cooled to 0° C. for 2 hours. Filtration provided 5.53 g of the desired product as colorless crystals which were used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645968B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-a6a0b2b8b8a94cf7962a2231c94cf5d5 |
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| Source note | uspto-grants-2003_11 |
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