HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444926Generated: October 25, 2026
p-Toluenesulfonic acid → HCID 58442369, compound
https://huagongshe.com/reaction/444926
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | Methyl 3-amino-6-bromo-5-(trifluoromethyl)picolinate | HCID 58964428 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58442369 | HCID 58442369 | — |
Reaction Steps
3-Amino-6-bromo-5-trifluoromethyl-pyridine-2-carboxylic acid methyl ester (Intermediate A4) (2 g, 6.69 mmol) was suspended in toluene (8 ml), and treated with p-toluenesulfonic acid (TsOH) (0.115 g, 0.669 mmol) and acetonylacetone (0.941 ml, 8.03 mmol). The reaction mixture was heated at reflux for 2 hours (using Dean-Stark apparatus) and allowed to cool to RT overnight. The resulting dark red/black solution was concentrated in vacuo to remove toluene and the crude residue diluted with EtOAc (200 ml), washed with NaHCO3 (50 ml), dried (MgSO4) and concentrated in vacuo to give a brown solid. Purification of the solid by chromatography on silica eluting with EtOAc/iso-hexane afforded the title compound; LC-MS Rt=5.58 min [M+H]+ 377/379 (Method 10 minLC_v002).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476269B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-c838c0491ae14cfeb76f34152d3ff06c |
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| Source note | uspto-grants-2013_07 |
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