Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Pentyn-2-ol | HCID 92915 | — |
| Reactant | 3-Cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester | HCID 67483447 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Catalyst | Iodide Ion | HCID 30165 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67483913 | HCID 67483913 | 92% |
Reaction Steps
A solution of 3-cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester (716 mg, 2.0 mmol) and triethylamine (2 mL, 0.01 mmol) in N,N-dimethylformamide (2 mL) was treated with 4-pentyne-2-ol (0.47 mL, 5.0 mmol). The resulting reaction mixture was degassed with argon and then treated with cooper iodide (10 mg, 0.05 mmol) and bis(triphenylphosphine)palladium (II) chloride (15 mg, 0.02 mmol). The reaction was then heated at 70° C. for 24 h. At this time, the reaction was cooled to 25° C. and concentrated in vacuo. The residue was diluted with ethyl acetate (40 mL) and a half-saturated aqueous sodium chloride solution (1×20 mL). The aqueous layer was back extracted with ethyl acetate (1×40 mL). The combined organic extracts were washed with a half-saturated aqueous sodium chloride solution (1×20 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60/40 ethyl acetate/hexanes) afforded 3-cyclopentyl-2-[4-(4-hydroxy-pent-1-ynyl)-phenyl]-propionic acid methyl ester (578 mg, 92%) as an amber oil: EI-HRMS m/e calcd for C20H26O3 (M+) 314.1881, found 314.1888.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06388071B2 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-60915239b2f14f60902f595d893251d2 |
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| Source note | uspto-grants-2002_05 |
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