HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036286Generated: November 1, 2026
(+-)-2-Butanol → Ethyl 2-(2'-fluoro-2,4'-bipyridin-5-yl)acetate
https://huagongshe.com/reaction/1036286
Participants
| Role | Name | HCID | Charge |
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| Reactant | (+-)-2-Butanol | HCID 6568 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Fluoropyridine-4-boronic acid | HCID 2783396 | — |
| Reactant | Ethyl 2-(6-chloropyridin-3-yl)acetate | HCID 15661146 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(2'-fluoro-2,4'-bipyridin-5-yl)acetate | HCID 58447698 | — |
Reaction Steps
To a flask containing ethyl 2-(6-chloropyridin-3-yl)acetate 208-1 (300 mg, 1.5 mmol), 2-fluoropyridin-4-ylboronic acid 205-4 (318 mg, 2.25 mmol), Pd(OAc)2 (17 mg, 0.075 mmoL), 2-dicyclohexylphosphino-2′,6′-dimethoxyybiphenyl (62 mg, 0.15 mmol), K3PO4 (800 mg, 9 mmol) under argon was added 2-butanol (1.5 mL). The reaction mixture was stirred at 100° C. for 10 hours. After cooled to room temperature, the mixture was diluted with ethyl acetate, washed with water and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude was purified by silica gel flash chromatography, eluted with 40% ethyl acetate in dichloromethane to give ethyl 2-(2′-fluoro-2,4′-bipyridin-5-yl)acetate 208-2 as a yellow solid. MS m/z 261.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546396B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-b8cf8103d64648ecafda12dea2503dc3 |
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| Source note | uspto-grants-2013_10 |
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