HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249146Generated: November 1, 2026
4-Chlorophenol → 1-(4-Chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-one
https://huagongshe.com/reaction/1249146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-3-methyl-3-trifluoromethylthio-butan-2-one | HCID 13117301 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(4-Chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-one | HCID 13117302 | 73% |
Reaction Steps
26 g (0.21 mol) of 4-chlorophenol and 42 g (0.3 mol) of potassium carbonate were introduced into 250 ml of acetone. 53 g (0.2 mol) of 1-bromo-3-methyl-3-trifluoromethylthio-butan-2-one in 50 ml of acetone were slowly added dropwise to the mixture, under reflux. After the end of the addition, the mixture was stirred under reflux for 12 hours and was filtered, and the filtrate was concentrated. The residue was taken up in 500 ml of methylene chloride, the solution was extracted by shaking with water and sodium bicarbonate solution, and the organic phase was dried over sodium sulphate and concentrated. The residue was distilled in vacuo. 45.3 g (73% of theory) of 1-(4-chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-one of boiling point 105° C./0.4 mbar were obtained. ##STR14##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04629732 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-ea417a378649483ba1547893643a1a22 |
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| Source note | uspto-grants-1986_12 |
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