HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993140Generated: November 2, 2026
Methyl Ethyl Ketone → HCID 67059668, compound
https://huagongshe.com/reaction/1993140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Difluorophenol | HCID 80879 | — |
| Reactant | 2-Butene, 1-bromo- | HCID 122414 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67059668 | HCID 67059668 | — |
Reaction Steps
122 g of anhydrous potassium carbonate was added to a 2-butanone (600 mL) solution containing 77.2 g of 2,3-difluorophenol, and then 90.0 mL of 1-bromo-2-butene (E/Z ratio=92/8) was added thereto. The solution was heated under reflux for 4 hours, then cooled to room temperature, and water was added dropwise thereto to stop the reaction. Extraction was performed with hexane (three times), and the collected organic phase was washed with 3M hydrochloric acid, water, saturated aqueous solution of sodium hydrogencarbonate, and saturated saline in this order, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure (155 to 160° C., 50 kPa), to thereby obtain 106 g of 1-(2-butenoxy)-2,3-difluorobenzene in the form of a colorless and transparent liquid (E/Z ratio=82/18 according to 1H-NM analysis).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07651630B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-23f31b27cdbf443f85c471f1fb9e9985 |
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| Source note | uspto-grants-2010_01 |
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