HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418055Generated: October 27, 2026
Water → Ethyl 4-(2,3-dimethylphenoxy)butyrate
https://huagongshe.com/reaction/418055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,3-Dimethylphenol | HCID 10687 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 4-(2,3-dimethylphenoxy)butyrate | HCID 57586544 | 94% |
Reaction Steps
To a solution of 2,3-dimethylphenol (25 g, 204 mmol) in DMSO (205 mL) was added 4-bromo-butyric acid ethyl ester (40.96 g, 210 mmol) and lithium hydride (2.0 g, 250 mmol) at room temperature. The resulting light brown solution was stirred for 2 days. Then, the reaction mixture was cooled to 0° C. and water (200 mL) was added slowly. The organic compound was extracted into hexanes (2×200 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 light brown oil. The crude mixture was purified by using a Biotage™ (40 L) column chromatography eluting with 5% ethyl acetate in hexanes to isolate 4-(2,3-dimethyl-phenoxy)-butyric acid ethyl ester (45.32 g, 94%) as a colorless oil: ES(+)-HRMS m/e calculated for C14H20O3 (M+)+ 236.1412, found 236.1419.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093253B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-ff810a13b7fc48fca2f099c25dc584b3 |
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| Source note | uspto-grants-2012_01 |
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