HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711242Generated: October 30, 2026
Toluene → Tert-butyl 5-(3-fluorophenyl)picolinate
https://huagongshe.com/reaction/711242
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Fluorophenylboronic acid | HCID 2733986 | — |
| Reactant | tert-Butyl 5-bromopyridine-2-carboxylate | HCID 24997839 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butyl 5-(3-fluorophenyl)picolinate | HCID 67208627 | — |
Reaction Steps
To a reaction flask was added tert-butyl 5-bromopicolinate 33-4 (516 mg, 2.00 mmol), 3-fluorophenylboronic acid 6-6 (280 mg, 2.00 mmol), Pd(PPh3)4 (140 mg, 0.20 mmol), toluene (10 mL), ethanol (2 mL) and 2M Na2CO3 (3 mL). The reaction mixture was bubbled with nitrogen for 2 minutes and stirred at 90° C. for 10 hours with the flask sealed. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (100 mL) and washed with saturated NaHCO3 aqueous solution, H2O and brine. The organic phase was dried over Na2SO4 and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, and eluted with 30% hexanes in ethyl acetate to give tert-butyl 5-(3-fluorophenyl)picolinate 33-5 as a white solid. MS m/z 274.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181235B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b7575e6a2afd41e2b9fe986ac056e729 |
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| Source note | uspto-grants-2015_11 |
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