Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | HCID 86595847 | HCID 86595847 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 69428901 | HCID 69428901 | — |
Reaction Steps
Into a mixture of trifluoro-methanesulfonic acid 4-ethylperoxymethyl-5-methyl-6-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-cyclohexa-1,5-dienyl ester (118.5 mg, 0.2219 mmol), Pd (PPh3)4 (6.4 mg, 0.025 eq.) and K3PO4 (70.7 mg, 1.5 eq.) in 1,4-dioxane (5 mL) was bubbled N2 for 10 min. To the reaction mixture was then added 4-methoxy benzene boronic acid (37.1 mg, 0.2441 mmol). The resulting mixture was heated to 8° C. for 16 h, filtered through a plug of silica gel, concentrated and purified on preparative TLC (10% MeOH/DCM) to yield 4-(4-methoxy-phenyl)-6-methyl-5-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-cyclohex-3-enecarboxylic acid ethyl ester as light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07183445B2 |
|---|
| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-c73194a1528e4fb5ac4b1cb832d3f97b |
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| Source note | uspto-grants-2007_02 |
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