Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67583627 | HCID 67583627 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67584014 | HCID 67584014 | 82% |
Reaction Steps
399 mg of the (2R,4R)-2-[2-{4-fluoro-2-[2-(4-fluoro-3-methoxyphenyl)ethyl]phenoxy}ethyl]-4-hydroxy-1-methylpyrrolidine [prepared as described in step (b) above] were dissolved in 5 ml of ethyl acetate. Addition of 0.38 ml of a 4N solution of hydrogen chloride in ethyl acetate resulted in the precipitation of crystals. The solvent was removed by evaporation under reduced pressure, and the resulting solid substance was dissolved in a small quantity (approximately 0.5 ml) of methylene chloride and then 5 ml of ethyl acetate were added to the resulting solution. The resulting mixture was then allowed to stand at room temperature for about 10 minutes. The crystals which precipitated were collected by filtration, and dried in vacuo, to give 359 mg (yield 82%) of the title compound as colorless crystals, melting at 128-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05843983 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-fad8d92633f3496ab6db301bfe0bdfb7 |
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| Source note | uspto-grants-1998_12 |
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