HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460020Generated: October 25, 2026
Benzyl Bromide → Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-
https://huagongshe.com/reaction/460020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-Hydroxy-3'-methylacetophenone | HCID 70135 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]- | HCID 12969325 | — |
Reaction Steps
A mixture of 4-hydroxy-3-methylacetophenone (5.0 g) in dry acetonitrile (50 ml) was treated with potassium carbonate (5.06 g) and benzyl bromide (3.96 ml) and the reaction mixture heated at 40° C. After 3 hours the reaction was allowed to cool and was concentrated. The residue was partitioned between water and ethyl acetate; the aqueous layer separated and extracted twice more with ethyl acetate. The organic solutions were combined and were dried with brine and over magnesium sulfate and concentrated to give the title compound as a colourless oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196107B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-da235d1cfd0447f28bdf62d1f7e867b5 |
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| Source note | uspto-grants-2007_03 |
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