HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382173Generated: October 31, 2026
Potassium Phosphate, Tribasic → Methyl 2-chloro-5-methylnicotinate
https://huagongshe.com/reaction/2382173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Methylboronic Acid | HCID 139377 | — |
| Reactant | Methyl 5-bromo-2-chloronicotinate | HCID 2763343 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | Methyl 2-chloro-5-methylnicotinate | HCID 11636946 | 87% |
Reaction Steps
To a solution of methyl 5-bromo-2-chloronicotinate (1.05 g, 4.19 mmol), K3PO4 (2.95 g, 13.90 mmol), methylboronic acid (0.32 g, 5.26 mmol) and tricyclohexylphosphine (0.11 g, 0.39 mmol) in toluene/water (16 ml/0.8 ml) under nitrogen atmosphere was added Pd(OAc)2 (0.04 g, 0.18 mmol). The mixture was heated at 100° C. overnight under nitrogen atmosphere. The reaction mixture was then cooled to room temperature and concentrated in vacuum. Ethyl acetate was added to the residue and this organic layer was washed with water, brine, dried over MgSO4, filtered and the solvent evaporated under vacuum to yield the desired product as a yellow oil. Yield=87%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258308B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-fed20cce1bcf4d6db64c93351143fcf6 |
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| Source note | uspto-grants-2012_09 |
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