HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573105Generated: October 25, 2026
Dimethylformamide → Methyl 2-(5-bromopyridin-3-yloxy)-4-fluorobenzoate
https://huagongshe.com/reaction/573105
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Bromo-5-hydroxypyridine | HCID 599529 | — |
| Reactant | Methyl 2,4-Difluorobenzoate | HCID 2782897 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(5-bromopyridin-3-yloxy)-4-fluorobenzoate | HCID 67227657 | — |
Reaction Steps
To a solution of 5-bromopyridin-3-ol (1.060 g) in 2-methyltetrahydrofuran (15 mL) was added potassium tert-butoxide (6.09 mL, 1.0M in tetrahydrofuran) dropwise. After stirring for 5 minutes, methyl 2,4-difluorobenzoate (1.049 g) was added as a solution in 2-methyltetrahydrofuran (2 mL) and the reaction was heated to 75° C. N,N-Dimethylformamide (2 mL) was added to the reaction and the reaction was stirred overnight. The reaction was cooled, diluted with ethyl acetate (100 mL) and washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (SF40-80) eluting with a gradient of 5% to 35% ethyl acetate/hexanes gave the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029404B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-4d177645839a45b0823d1cea560f7a46 |
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| Source note | uspto-grants-2015_05 |
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