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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534093Generated: October 30, 2026

4-Methoxymandelic acid → 2-Trimethylsilylethyl 4-methoxymandelate

https://huagongshe.com/reaction/1534093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxymandelic acidHCID 112056—
ReactantHCID 178457954HCID 178457954—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2-Trimethylsilylethyl 4-methoxymandelateHCID 1370572872%

Reaction Steps

To a solution of 4-methoxymandelic acid (2.00 g, 10.978 mmol) in 55 mL of dioxane at 90° C. is added 2-trimethylsilylethyl-N,N-diisopropyl-pseudourea. The resulting solution is refluxed for about 8 hours. After cooling the mixture is diluted with 50 mL of ethyl acetate, filtered, washed with saturated aqueous sodium bicarbonate followed by brine, dried over magnesium sulfate, and concentrated. The resulting residue is chromatographed on silica gel (9/1 hexanes/ethyl acetate) to give the title compound as an oil: 2.24 g, 72% yield. 1H NMR (300 MHz, CDCl3): 7.32 (d, J=8.8, 2 H), 6.89 (d, J=8.8, 2 H), 5.08 (d, J=5.6, 1 H), 4.38-4.17 (m, 2 H), 3.81 (s, 3 H), 3.41 (d, J=5.6, 1 H), 0.96 (m, 2 H), 0.01 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087631
Source datasetuspto-grants-1992_02
ORD IDord-037917923f3e438fbf6b7a03f3e88f07
Source noteuspto-grants-1992_02