Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | HCID 19361036 | HCID 19361036 | — |
| Reactant | 1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanol | HCID 58629822 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58629891 | HCID 58629891 | 34.2% |
Reaction Steps
A stirred solution of 1-{6-[4-(trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanol (62 mg, 0.20 mmol) and ethyl (2E)-3-(4-hydroxy-3,5-dimethylphenyl)-2-propenoate (79 mg, 0.36 mmol) in THF (4 mL) at 0° C. under nitrogen was added ADDP (101 mg, 0.40 mmol) followed by tri-N-butylphosphine (0.100 mL, 0.40 mmol). The resulting mixture was then allowed to warm slowly to ambient temperature overnight. After 66 h the solvent was removed under vacuum (Genevac) and the resulting solid partitioned between DCM (5 mL) and water (5 mL), the layers separated and the aqueous re-extracted with DCM (5 mL). The combined organic layer was then reduced under vacuum and purified by SPE (silica, 10 g cartridge) eluting with cyclohexane:EtOAc (gradient 20:1 to 1:1) to give the title compound (35 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07338960B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-1938df07b3d3446c92b428ddfd36ba34 |
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| Source note | uspto-grants-2008_03 |
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