HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197646Generated: October 30, 2026
4-Hydroxybenzaldehyde → HCID 86611514, compound
https://huagongshe.com/reaction/2197646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86611514 | HCID 86611514 | 36% |
Reaction Steps
To a solution of 4-hydroxy benzaldehyde (4.22 g, 34.6 mmol) and 2,5-dibromopyridine (8.19 g, 34.6 mmol) in dimethylacetamide (100 mL) is added K2CO3 (11.95 g, 86.4 mmol) at RT. The reaction mixture is warmed to 130° C. for 8 h. The reaction mixture is then poured into H2O (200 mL) and saturated NaHCO3 (100 mL), extracted with EtOAc (3×200 mL), and then the combined extracts are washed with saturated NaHCO3, brine, dried over MgSO4, filtered, and concentrated. The mixture is loaded on silica gel, eluted with hexanes with a gradient from 5% of ethyl acetate to 25% of ethyl acetate giving ethyl 4-(5-Bromo-pyridin-2-yloxy)-benzaldehyde (3.50 g, 36%) as a white solid. 1NMR (400 MHz, CDCl3) δ ppm: 9.96 (s, 1H), 8.23 (d, J=2.6 Hz, 1H), 7.93-7.90 (m, 2H), 7.83 (ds, J=2.6, 8.4 Hz, 1H), 7.27-7.24 (m, 2H), 6.92 (d, J=7.9 Hz, 1H); MS (ES): [M+H]+ found 277.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338611B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-b41f1de7cee04fdb98af8592476fdda0 |
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| Source note | uspto-grants-2012_12 |
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