Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 70153550 | HCID 70153550 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Product | HCID 18723505 | HCID 18723505 | — |
Reaction Steps
A solution of 0.062 g (0.14 mmol) of Ph3Bi (Aldrich in 1 mL of CH2Cl2 and 0.65 mL of THF at rt was added 0.027 mL (0.18 mmol) of trifluoroacetic acid and the reaction mixture was stirred for 10 min. This solution was added to a solution of 0.046 g (0.1 mmol) of 1-(1-naphthoyl)-3-(RS)-(4-(4-fluorophenyl)piperidinylmethyl)-4-(SR)-hydroxyethylpyrrolidine in 1 mL of CH2Cl2. To this reaction mixture was added 0.0083 g (0.046 mmol) of Cu(OAc)2 and the reaction mixture was stirred at 40° C. for 72 h. The reaction mixture was filtered through a thin pad of silica (acetone: hexanes, 1:2) and the filtrate was concentrated. The residue was purified by chromatography (silica, Waters RCM 25×100 with (0.1% iPr2NH in methyl tbutyl ether): hexane=2.25:7.0) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489354B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-e8721f9496cb45968d80ef9d1b598d3a |
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| Source note | uspto-grants-2002_12 |
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