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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670060Generated: November 1, 2026

Water → Ethyl 4-(2,3-dimethylphenoxy)butyrate

https://huagongshe.com/reaction/1670060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,3-DimethylphenolHCID 10687—
ReactantLithium hydrideHCID 62714—
ReactantEthyl 4-bromobutyrateHCID 76300—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 4-(2,3-dimethylphenoxy)butyrateHCID 5758654494%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989454B2
Source datasetuspto-grants-2011_08
ORD IDord-834a2de8dc1342bf87a39444739fa9e3
Source noteuspto-grants-2011_08