HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35417Generated: October 25, 2026
Hydrochloric Acid → 4-Chloro-2-fluoro-5-isopropoxy-nitrobenzene
https://huagongshe.com/reaction/35417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Chloro-2-fluoro-5-isopropoxy-nitrobenzene | HCID 13108986 | 91.3% |
Reaction Steps
To a stirred solution of 15.8 g (0.083 mole) of 2-chloro-4-fluoro-5-nitrophenol in 90 mL of acetone was added 17.1 g (0.12 mole) of potassium carbonate followed by a solution of 21.0 g (0.12 mole) of 2-iodopropane in 10 mL of acetone. After complete addition, the reaction mixture was heated at 60° C. for approximately 18 hours. The mixture was cooled and poured into a mixture of ice and concentrated hydrochloric acid. The resultant mixture was extracted with ethyl acetate, and the extract was washed with a 1N sodium hydroxide solution. The washed extract was dried over anhydrous magnesium sulfate and was filtered. The solvent was evaporated under reduced pressure to leave 17.7 g of 4-chloro-2-fluoro-5-(1-methylethoxy)nitrobenzene as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766233 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-6a1d1b7f41cc4078a574d6eee7881fa9 |
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| Source note | uspto-grants-1988_08 |
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