HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503140Generated: October 29, 2026
4-Fluorophenol → 1-(2,2-Diethoxyethoxy)-4-fluorobenzene
https://huagongshe.com/reaction/503140
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(2,2-Diethoxyethoxy)-4-fluorobenzene | HCID 11447518 | — |
Reaction Steps
To a solution of 10.0 g of 4-fluorophenol and 16.1 ml of bromoacetaldehyde diethylacetal in 100 ml dimethylformaldehyde was added 18.5 g of potassium carbonate at room temperature, and the mixture was stirred at 120° C. for two days. The reaction mixture was filtered through Celite, and the filtrate was diluted with ethyl acetate. The organic layer was sequentially washed with saturated aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=0:10 to 1:20), to give 17.3 g of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776890B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-9b798ee227b84dec8d4c1654f51162f5 |
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| Source note | uspto-grants-2010_08 |
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