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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266476Generated: October 27, 2026

tert-Butanol → 2-(4-methanesulfonylbenzyl)-3-oxobutyric Acid Ethyl Ester

https://huagongshe.com/reaction/2266476

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantEthyl AcetoacetateHCID 8868—
Reactant4-(Methylsulfonyl)benzyl BromideHCID 2733581—
ReactantPotassium tert-butoxideHCID 23665647—
SolventCitric AcidHCID 311—
SolventTetrahydrofuranHCID 8028—
Product2-(4-methanesulfonylbenzyl)-3-oxobutyric Acid Ethyl EsterHCID 68780413—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of potassium tert-butoxide (4.5 g) in anhydrous tetrahydrofuran (70 mL) at 0° C. was treated with a mixture of tert-butanol (0.2 mL) and 3-oxobutyric acid ethyl ester (5.2 g). After stirring at 15° C. for 15 minutes a solution of 1-bromomethyl-4-methanesulfonylbenzene (10 g) in tetrahydrofuran (30 mL) was added and the resulting mixture heated at 70° C. for 17 hours. The mixture was diluted with saturated aqueous citric acid solution (20 mL) and extracted with ethyl acetate. The combined extracts were washed with saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of pentane and dichloromethane (2:1 to 0:1 by volume) to afford title compound as a gum, 3.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858640B2
Source datasetuspto-grants-2010_12
ORD IDord-d355b4c00d4b4742af19560c8ee8cc27
Source noteuspto-grants-2010_12