HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632452Generated: October 25, 2026
Hydrochloric Acid → 5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acid
https://huagongshe.com/reaction/632452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Potassium cyclopropyltrifluoroborate | HCID 23697338 | — |
| Reactant | 5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acid | HCID 71087582 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Butyl-1-adamantylphosphine | HCID 68995490 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acid | HCID 71087435 | 79% |
Reaction Steps
5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acid (2 g, 6.37 mmol), potassium cyclopropyltrifluoroborate (952 mg, 6.43 mmol), cesium carbonate (6.22 g, 19.1 mmol) and palladium(II)acetate (28.6 mg, 127 μmol) were suspended in toluene (55 mL) and water (6.11 mL) under an argon atmosphere. Butyl-1-adamantylphosphin (68.5 mg, 191 μmol) was added, the reaction mixture was heated to 120° C. for 1 d, poured onto icewater/1N HCl (150 mL) and extracted with EtOAc (2×300 mL). The combined organic layers were washed with icewater/brine (150 mL), dried over Na2SO4 and concentrated in vacuo to give the title compound (1.38 g, 79%) as a yellow solid. MS (EI): m/e=276.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321727B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-ae0dddf6dcb44928a58fb06af65a7bda |
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| Source note | uspto-grants-2016_04 |
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