HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338570Generated: October 26, 2026
Potassium Carbonate → Tert-butyl 3-(3-methylpyridin-4-yl)benzoate
https://huagongshe.com/reaction/338570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-3-methylpyridine | HCID 2757709 | — |
| Reactant | (3-((Tert-butoxy)carbonyl)phenyl)boronic acid | HCID 2773299 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Tert-butyl 3-(3-methylpyridin-4-yl)benzoate | HCID 57895121 | 71.4% |
Reaction Steps
4-Chloro-3-methylpyridine (2.00 g, 15.7 mmol), 3-(tert-butoxycarbonyl)phenylboronic acid (5.42 g, 24.4 mmol), a 2M aqueous solution of potassium carbonate (31.4 mL, 62.8 mmol), and palladium tetrakis(triphenylphosphine) (Pd(PPh3)4, 0.906 g, 0.784 mmol) were suspended in 1,2-dimethoxyethane (DME, 150 mL). The resulting mixture was stirred and heated to 80° C. for 60 hours. The crude reaction mixture was cooled to room temperature and then the layers were separated. The organic layer was evaporated to dryness and then purified on 120 g of silica gel utilizing a gradient of 0-70% ethyl acetate in hexanes to yield the pure product as a pale yellow oil (3.02 g, 11.2 mmol, 71.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889875B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ad087937869e45669e753b6ee4cfb5c9 |
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| Source note | uspto-grants-2014_11 |
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