HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746073Generated: November 2, 2026
Potassium Fluoride → HCID 90413471, compound
https://huagongshe.com/reaction/1746073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Methyl 4-amino-3,6-dichloro-5-fluoropicolinate | HCID 22677265 | — |
| Reactant | HCID 53217346 | HCID 53217346 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 90413471 | HCID 90413471 | 68.7% |
Reaction Steps
Methyl 4-amino-3,6-dichloro-5-fluoropicolinate (1.5 g, 6.28 mmol), 2-(benzo[d][1,3]dioxol-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.024 g, 8.16 mmol), potassium fluoride (0.875 g, 15.06 mmol; Note: Related examples utilize cesium fluoride) and bis(triphenylphosphine)palladium(II)chloride (0.440 g, 0.628 mmol) were combined in acetonitrile (13 mL) and water (4.5 mL). The reaction mixture was then irradiated in a microwave at 110° C. in a capped vial for 20 min, with external IR-sensor temperature monitoring from the side of the vessel. The cooled reaction mixture was partitioned between ethyl acetate and water. The organic phase was dried and concentrated onto 1.2 g of silica gel. This mixture was applied to the top of a silica gel column and the product was eluted with a 7-60% hexane/ethyl acetate gradient solvent system to provide the title compound as a white solid (1.4 g, 68.7%): mp 146-148° C.; 1H NMR (400 MHz, CDCl3) δ 7.16-7.09 (m, 1H), 6.98-6.85 (m, 2H), 6.01 (s, 2H), 4.91 (br s, 2H), 3.98 (s, 3H); ESIMS m/z 325 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09149038B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-cbaaef7a0f42428a9a13a71e4da12963 |
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| Source note | uspto-grants-2015_10 |
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