HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192701Generated: October 26, 2026
Methanol → 1-[4-(4-Bromo-2-fluorobenzyloxy)-2-hydroxyphenyl]ethanone
https://huagongshe.com/reaction/2192701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 2',4'-Dihydroxyacetophenone | HCID 6990 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-fluorobenzyl bromide | HCID 2733660 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[4-(4-Bromo-2-fluorobenzyloxy)-2-hydroxyphenyl]ethanone | HCID 66988238 | 75.4% |
Reaction Steps
1-(2,4-dihydroxyphenyl)ethanone (25.3 g, 0.17 mol) and 4-bromo-1-bromomethyl-2-fluorobenzene (44.6 g, 0.17 mol) were dissolved in DMF (150 mL). Potassium carbonate (11.8 g, 0.09 mol) was added to the solution under ice-cooled conditions, and the mixture was stirred under ice-cooled conditions and further stirred at room temperature for 12 hours. Again, potassium carbonate (11.8 g, 0.09 mol) was added to the mixture under ice-cooled conditions, and the mixture was stirred under ice-cooled conditions for 30 minutes and further stirred at room temperature for 12 hours. Methanol (100 mL) was added to this reaction solution, and the mixture was stirred at 80° C. for 1 hour. Thereafter, water (150 mL) was added to the mixture, and precipitated crystals were filtered and washed with methanol. The crystals were vacuum-dried at 60° C. for 2 hours, yielding 1-[4-(4-bromo-2-fluorobenzyloxy)-2-hydroxyphenyl]ethanone (43.5 g, yield: 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329739B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-007942aad0dc467980dae15584f6932f |
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| Source note | uspto-grants-2012_12 |
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