HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370458Generated: October 30, 2026
4-Nitrophenol → 1-(4-Nitrophenoxy)propan-2-one
https://huagongshe.com/reaction/370458
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(4-Nitrophenoxy)propan-2-one | HCID 308507 | 88.6% |
Reaction Steps
A mixture consisting of 35 g of 4-nitrophenol, 35 g of chloroacetone, 35 g of potassium carbonate, 1 g of potassium iodide and 500 ml of acetone was heated at reflux with stirring for 3 hr. Reaction mixture was concentrated underd reduced pressure; the concentrate was extracted with ethyl acetate; the ethyl acetate layer was washed consecutively with 5% aqueous solution of sodium hydroxide, water and saturated saline; and dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure; the residue was dissolved in 300 ml of ethanol, added with 100 ml of n-hexane; and subsequently left standing overnight at room temperature. Yellow crystals thus isolated were filtered off, dried and yielded 43.5 g of 4-nitrophenoxyacetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04526893 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-d78bc5fb6d944318868a006df69293e8 |
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| Source note | uspto-grants-1985_07 |
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