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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395944Generated: October 30, 2026

Ethyl isobutyrate → ethyl 4-chloro-2,2-dimethylbutyrate

https://huagongshe.com/reaction/2395944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isobutyrateHCID 7342—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productethyl 4-chloro-2,2-dimethylbutyrateHCID 10797430—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 22.2 ml of diisopropylamine in 150 ml of tetrahydrofuran being stirred, 93.6 ml of a 1.6 M solution of n-butyl lithium in hexane was added at -5° to 0° C., followed by stirring for 30 minutes. After the reaction mixture was cooled to -78° C. and 19.0 ml of ethyl isobutyrate was added dropwise to the mixture and stirred for 45 minutes. A solution of 11.9 ml of 1-bromo-2-chloroethane in 10 ml of tetrahydrofuran was added dropwise to the reaction mixture. After the reaction mixture was stirred at -78° C. for 1 hour and then at roomtemperature (15° to 20° C.) for 2 hours, an excess amount of an aqueous solution of ammonium chloride was added, followed by extractionwith ethyl acetate. After the extract was washed with water and dried over MgSO4, the solvent was distilled off; the residue was then distilled under reduced pressure, to yield 24.7 g of the title compound in the form of a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491145
Source datasetuspto-grants-1996_02
ORD IDord-6788a144a8f145d0899ed1b1e9de313d
Source noteuspto-grants-1996_02