HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889639Generated: October 27, 2026
Hydrogen Bromide → 3-(4-Bromo-2-fluoro-phenoxy)-2,6-dimethyl-pyridine
https://huagongshe.com/reaction/889639
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 4-(2,6-Dimethyl-pyridin-3-yloxy)-3-fluoro-phenylamine | HCID 59287321 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Bromo-2-fluoro-phenoxy)-2,6-dimethyl-pyridine | HCID 59287311 | 89% |
Reaction Steps
A solution of sodium nitrite (4.57 g, 66.3 mmol) in water (75 ml) was added dropwise (over 45 minutes) to a cooled (at 0° C.) solution of intermediate D15 (7.7 g, 33.2 mmol) in 48% aqueous HBr (75 ml). The reaction mixture was warmed to room temperature and further stirred for 15 minutes, after which it was cooled again to 0° C. and copper(I) bromide (7.31 g, 49.8 mmol) was added portionwise. The mixture was allowed to reach room temperature, stirred for 15 minutes and finally it was heated at 140° C. for 1.5 hours. The reaction mixture was cooled to room temperature and neutralized with an aqueous saturated solution of potassium carbonate. EtOAc was added, the organic layer was separated and washed with brine, dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-10% EtOAc/heptane as eluent). The desired fractions were collected and evaporated in vacuo to yield D16 (8.75 g, 89%) as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252937B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-e6c2ba6a655b4b4c920e6f84f0c1a746 |
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| Source note | uspto-grants-2012_08 |
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