HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51911Generated: October 25, 2026
2-Chloro-5-(trifluoromethyl)pyridine → 2-(5-Trifluoromethyl-pyridin-2-yl)-benzoic acid isopropyl ester
https://huagongshe.com/reaction/51911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-(trifluoromethyl)pyridine | HCID 92342 | — |
| Reactant | (2-(Isopropoxycarbonyl)phenyl)boronic acid | HCID 53435142 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(5-Trifluoromethyl-pyridin-2-yl)-benzoic acid isopropyl ester | HCID 69891295 | 70% |
Reaction Steps
2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713489B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-3da357480ed243f08b79952da60fad6e |
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| Source note | uspto-grants-2004_03 |
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