HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948679Generated: October 31, 2026
Bromomethyl 4-methoxyphenyl ketone → HCID 887806, compound
https://huagongshe.com/reaction/1948679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 887806 | HCID 887806 | 96.1% |
Reaction Steps
24 g of potassium carbonate are added to a solution of 20 g (0.115 mol) of 4-bromophenol and 26.5 g (0.115 mol) of 2-bromo-4′-methoxyacetophenone in 400 of acetonitrile, and the reaction mixture is heated under reflux for five hours. The precipitate is subsequently filtered off, the filtrate is evaporated to dryness, the residue is taken up in 10 ml of water, and the aqueous solution is extracted twice with 10 ml of ethyl acetate each time. The combined organic phases are washed with 10 ml of saturated sodium chloride solution and dried over sodium sulfate. After the solvent has been stripped off, the residue is triturated with 50 ml of diethyl ether, and the resultant crystalline product is filtered off with suction in vacuo, giving 35.5 g of 2-(4-bromophenoxy)-1-(4-methoxyphenyl)ethanone as beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399509B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-0943355fad0e42cf85017c39819d9a0a |
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| Source note | uspto-grants-2013_03 |
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