HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592130Generated: October 25, 2026
Toluene → Ethyl 2-(4-(2-methylpyridin-4-yl)phenyl)acetate
https://huagongshe.com/reaction/592130
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl (4-iodophenyl)acetate | HCID 14974990 | — |
| Reactant | 2-Methylpyridine-4-boronic acid pinacol ester | HCID 16414274 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(4-(2-methylpyridin-4-yl)phenyl)acetate | HCID 58447956 | — |
Reaction Steps
To a sealed tube were added 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (2.2 g, 10 mmol), ethyl 2-(4-iodophenyl)acetate 26-1 (2.9 g, 10 mmol), Pd(PPh3)4 (0.231 g, 0.2 mmol), toluene (30 mL), ethanol (10 mL) and 2M Na2CO3 (10 mL). The reaction mixture was flushed with nitrogen and stirred at 90° C. for 10 hours. After cooled down to room temperature, the reaction mixture was diluted into 200 mL ethyl acetate and washed with saturated sodium bicarbonate solution and then brine. The organic phase was dried over Na2SO4 and then taken to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 50% ethyl acetate in hexane to give ethyl 2-(4-(2-methylpyridin-4-yl)phenyl)acetate 26-2 as an oil. MS m/z 256.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238646B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-12ecdbc9d793437094f0f3e0fb79a32f |
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| Source note | uspto-grants-2016_01 |
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