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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266565Generated: October 26, 2026

tert-Butanol → 2-(2,4-dichlorobenzyl)-3-oxopentanoic Acid Methyl Ester

https://huagongshe.com/reaction/2266565

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantMethyl 3-oxovalerateHCID 121699—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(2,4-dichlorobenzyl)-3-oxopentanoic Acid Methyl EsterHCID 68781491—

Reaction Steps

A suspension of potassium tert-butoxide (8.4 g) in anhydrous tetrahydrofuran (180 mL) at 0° C. was treated with a mixture of tert-butanol (0.4 mL) and 3-oxopentanoic acid methyl ester (9.8 g). After stirring at room temperature for 30 minutes a solution of 2,4-dichloro-1-chloromethylbenzene (14.7 g) in tetrahydrofuran (20 mL) was added and the resulting mixture warmed to room temperature and then stirred at this temperature for 6 days. The mixture was diluted with water (200 mL), extracted with ethyl acetate and the combined extracts washed with water and saturated aqueous sodium chloride solution and then 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 (1:0 to 1:1 by volume) to afford title compound as a white solid, 7.0 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858640B2
Source datasetuspto-grants-2010_12
ORD IDord-7ba2c4844f9a4e88b3f99dc00193cfaf
Source noteuspto-grants-2010_12