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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274285Generated: October 29, 2026

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

https://huagongshe.com/reaction/274285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isobutyrateHCID 7342—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
SolventTetrahydrofuranHCID 8028—
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 was added 93.6 ml of 1.6M n-butyllithium-hexane with stirring at -5° to 0° C. and the mixture was stirred for 30 minutes. The reaction mixture was cooled to -78° C. and 19.0 ml of ethyl isobutyrate was added dropwise. The mixture was then further stirred for 45 minutes, after which a solution of 11.9 ml of 1-bromo-2-chloroethane in 10 ml of tetrahydrofuran was added dropwise. The reaction mixture was stirred at -78° C. for 1 hour and, then, at room temperature for 2 hours. After an excess amount of an aqueous solution of ammonium chloride was added, the mixture was extracted with ethyl acetate. The extract was washed with water and dried (MgSO4) and the solvent was distilled off. Finally, the residue was distilled under reduced pressure to provide 24.7 g of the title compound as colorless oil. b.p. 54°-56° C./0.25 mmHg

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389633
Source datasetuspto-grants-1995_02
ORD IDord-d14a21dacd524020aba072abd67a3de3
Source noteuspto-grants-1995_02