Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-tert-Butylphenylboronic acid | HCID 2734320 | — |
| Reactant | 2-(3-Bromo-phenyl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester | HCID 67442831 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67441426 | HCID 67441426 | 49.2% |
Reaction Steps
A mixture of 2-(3-bromo-phenyl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.50 g, 1.29 mmol), 4-tert-butylbenzeneboronic acid (0.46 g, 2.58 mmol), bis(triphenylphosphine)palladium (II) chloride (91 mg, 0.13 mmol) and 2 M sodium carbonate (1.3 mL, 2.6 mmol) in dioxane (5 mL) was heated for 3 hours at 120° C. After cooling to room temperature, the mixture was treated with ethyl acetate (50 mL) and washed with water (20 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. Purification on flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company)(10% ethyl acetate/hexanes) to afford 2-(4′-tert-butyl-biphenyl-3-yl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.28 g, 49%) as a white solid: LC/MS m/e calcd for C30H35NO2 (M+H)+: 442.6, observed: 442.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08586747B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-a4fdb47e427b43378b25091b28d4fa4e |
|---|
| Source note | uspto-grants-2013_11 |
|---|