Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzyl bromide | HCID 122573 | — |
| Reactant | HCID 69889515 | HCID 69889515 | — |
| Solvent | 2-Methylpentane | HCID 7892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86586772 | HCID 86586772 | 62.3% |
Reaction Steps
Sodium hydride (60% in oil, 100 mg, 2.5 mmol) was washed twice with iso-hexane and added as a suspension in THF (3 ml) to a stirred mixture of (1R*,2R*,5S*,6S*)-8-benzyl-6-ethoxycarbonyl-6-fluoro-1-phenyl-8-azabicyclo[3.2.1]octan-2-ol (Description 38; 512 mg, 1.3 mmol), 3,5-bis(trifluoromethyl)benzyl bromide (0.5 ml, 2.7 mmol), 18-crown-6 (360 mg, 1.37 mmol) in THF (5 ml) at room temperature. The reaction mixture was stirred for 40 hours, quenched with saturated aqueous NH4Cl and extracted into a 1:1 mixture of iso-hexane:diethyl ether. The combined organic extracts were washed with water, dried (Na2SO4) and concentrated. The residue was purified by chromatography on silica gel (iso-hexane:diethyl ether) to give the title compound (494 mg, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727249B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-dcd71f30d1fb4dddb7cef42ad39e3372 |
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| Source note | uspto-grants-2004_04 |
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