HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255937Generated: October 31, 2026
Potassium Carbonate → 1-(2,3-Dichloro-4-butyrylphenoxy)cyclobutane-1-carboxylic acid
https://huagongshe.com/reaction/255937
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 1-bromocyclobutanecarboxylate | HCID 97595 | — |
| Reactant | 1-(2,3-Dichloro-4-hydroxyphenyl)butan-1-one | HCID 14099856 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2,3-Dichloro-4-butyrylphenoxy)cyclobutane-1-carboxylic acid | HCID 20148698 | — |
Reaction Steps
A mixture of 2,3-dichloro-4-butyrylphenol (7 g, 0.03 mole), ethyl 1-bromocyclobutanecarboxylate (10.23 g, 0.049 mole) and potassium carbonate (7.5 g, 0.054 mole) in N,N-dimethylformamide (60 ml) was stirred and heated at 65° C. for 18 hours. The reaction mixture was poured into ice water and the resulting mixture was extracted with ether. The ether extract was washed with a 1% sodium hydroxide solution, then with water and finally dried over MgSO4. The ether was evaporated in vacuo and the residue treated with acetic acid (60 ml) and 5% hydrochloric acid (15 ml). The mixture was stirred and refluxed overnight. The solvents were evaporated in vacuo. The residue was chromatographed over a column containing silica gel (140 g) using methylene chloride/tetrahydrofuran/acetic acid 50/1/1 as the eluent. The pertinent fractions were united, treated with toluene and evaporated in vacuo to obtain 1-(2,3-dichloro-4-butyrylphenoxy)cyclobutane-1-carboxylic acid as a liquid whose identity was confirmed by NMR and purity by thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04699926 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-73cd8f7c18c04b6f96cb517683a466ec |
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| Source note | uspto-grants-1987_10 |
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