HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388554Generated: October 30, 2026
Water → 4-Chloro-2-fluoro-5-isopropoxy-nitrobenzene
https://huagongshe.com/reaction/1388554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Chloro-2-fluoro-5-isopropoxy-nitrobenzene | HCID 13108986 | 57.9% |
Reaction Steps
To a solution of 2-chloro-4-fluoro-5-nitrophenol (19.1 g) in acetonitrile (100 ml), there was added anhydrous potassium carbonate (8 g). After stirring at room temperature for several minutes, isopropyl iodide (25 g) was added thereto, and the resultant mixture was heated under reflux for 3 hours. After being allowed to cool to room temperature, water was added thereto, and the reaction mixture was extracted with ether. The ether extract was washed with a 5% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium sulfate and subjected to filtration. The filtrate was concentrated under reduced pressure, and the residue was recrystallized from ethanol to obtain 13.5 g of 4-chloro-2-fluoro-5-isopropoxynitrobenzene. M.P., 61.3°-62.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04431822 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-04633ca82b394acba632dd2648e7032b |
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| Source note | uspto-grants-1984_02 |
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