Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 3-(2-Bromoethoxy)-5-phenylisoxazole | HCID 19596487 | — |
| Product | HCID 19596453 | HCID 19596453 | 82% |
Reaction Steps
Pyrrolidine (710 mg) was added to 3-(2-bromoethoxy)-5-phenylisoxazole (268 mg), and the mixture was stirred at 100° C. for one hour. After ice-cold water (20 ml) was added to the reaction mixture and the mixture was extracted with ether (20 ml×2), the organic layer was dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate) to obtain the title compound (211 mg, 82%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005116 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-b0703361af6d478d83baea8cdb18c74f |
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| Source note | uspto-grants-1999_12 |
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