HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420341Generated: October 26, 2026
Potassium Persulfate → 4-(2-Formyl-3-methyl-phenoxy)-butyric acid ethyl ester
https://huagongshe.com/reaction/420341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Ethyl 4-(2,3-dimethylphenoxy)butyrate | HCID 57586544 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2-Formyl-3-methyl-phenoxy)-butyric acid ethyl ester | HCID 57586453 | 205.6% |
Reaction Steps
A mixture of copper(II)sulfate pentahydrate (21.98 g, 88.06 mmol) and potassium persulfate (71.42 g, 264 mmol) in water (396 mL) was heated to 63-65° C. to obtain a blue colored solution. Then, a solution of 4-(2,3-dimethyl-phenoxy)-butyric acid ethyl ester (20.81 g, 88.06 mmol) in acetonitrile (220 mL) was added at the above temperature. The resulting light green solution was refluxed for 40 minutes. Then, the reaction mixture was cooled to ˜5° C. in order to precipitate most of the inorganic solids. The resulting solids were collected by filtration and the solid cake was washed with dichloromethane (1.0 L). The two layers of filtrate were separated and the aqueous layer was extracted with dichloromethane (200 mL). The combined organic extracts were washed with brine solution (150 mL) and the organic solution was dried over anhydrous magnesium sulfate. Filtration of the drying agent and the removal of the solvent gave a brown oil. The crude mixture was purified by using a Biotage (40L) column chromatography eluting with 5-10% ethyl acetate in hexanes to obtain 4-(2-formyl-3-methyl-phenoxy)-butyric acid ethyl ester (45.32 g, 94%) as a colorless oil: EI(+)-HRMS m/e calculated for C14H18O4 (M+)+ 250.1205, found 250.1202.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093385B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0f5f8cfcf30546de8c6fa57763472990 |
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| Source note | uspto-grants-2012_01 |
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