HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642971Generated: October 25, 2026
Water → 1-(4-(Methoxymethyl)phenyl)ethan-1-one
https://huagongshe.com/reaction/642971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-(Methoxymethyl)phenyl)ethan-1-one | HCID 89590 | 31% |
Reaction Steps
To a mixture of 4′-bromoacetophenone (300 mg, 1.51 mmol) and 1,4-dioxane (4 ml) were added water (0.4 ml), cesium carbonate (1.48 g, 4.54 mmol), potassium methoxymethyl trifluoroborate (459 mg, 3.02 mmol) and 1′,1′-bis(diphenylphosphino)ferrocenedichloropalladium (II) (110 mg, 0.151 mmol). Then, the reaction mixture was stirred at 100° C. (external temperature) for 7 hours. After the reaction mixture was cooled at room temperature, water and methylene chloride were added to the mixture, followed by filtration using Celite. The separated organic layer was washed with an aqueous saturated sodium chloride solution. The organic layer was separated, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (heptane/ethyl acetate) to obtain the title compound (76 mg, 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696347B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-373428bdf8fe45029c3b397c373b8980 |
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| Source note | uspto-grants-2010_04 |
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