関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6-Bromopyridine-2-carboxylic acid | HCID 593919 | — |
| 反応物 | 1-Cyclohexenylboronic acid | HCID 3862902 | — |
| 触媒 | HCID 178418807 | HCID 178418807 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 6-Cyclohexenyl-pyridine-2-carboxylic acid | HCID 71087233 | 61.2% |
反応手順
Under an atmosphere of nitrogen, a solution of 6-bromo-pyridine-2-carboxylic acid (CAN 1190-87-4, 3 g, 6.4 mol), cyclohexenylboronic acid (CAN 21190-87-4, 0.89 g, 7.1 mmol), 1,1′-bis(diphenyl-phosphino)ferrocene-palladium(II)dichloride methylene chloride complex (CAN 95464-05-4, 8 mg, 0.13 mmol), potassium carbonate (1.78 g, 12.9 mmol) in H2O (30 mL) was heated to 100° C. overnight. The reaction mixture was extracted with ethyl acetate (50 mL). The pH of the aqueous layer was adjusted to 5 by addition of 1 N hydrochloric acid and the resulting mixture was extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with water and brine, dried over anhydrous sodium sulfate and evaporated. The residue was purified by prep-HPLC to yield the title compound (0.8 g, 3.94 mmol, 61.2%) as yellow oil; MS (EI): m/e=204.2 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09290451B2 |
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| 出典データセット | uspto-grants-2016_03 |
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| ORD ID | ord-7985a38b8bfa4040a747141ca1ca774c |
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| 出典メモ | uspto-grants-2016_03 |
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