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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296048Generated: October 31, 2026

Ethyl isobutyrate → 2,2-Dimethyl-3-[4-(3-pyridylmethyl)phenyl]propionic acid ethyl ester

https://huagongshe.com/reaction/2296048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isobutyrateHCID 7342—
ReactantBenzyl ChlorideHCID 7503—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventHexamethylphosphoramideHCID 12679—
Product2,2-Dimethyl-3-[4-(3-pyridylmethyl)phenyl]propionic acid ethyl esterHCID 54391330—

Reaction Steps

To a 3.0 M solution of lithium diisopropylamide in tetrahydrofuran [prepared from diisopropylamine (0.56 ml), tetrahydrofuran (5 ml) and a 1.4 M solution of butyllithium in hexane (2.2 ml)] was added dropwise 0.41 ml of ethyl isobutyrate at -70° C., and the mixture was stirred at that temperature for 40 minutes. To it was added dropwise a solution of 0.26 g of the benzyl chloride compound (prepared as described in Reference Example 2) in 2.8 ml of a mixture of HMPA and tetrahydrofuran (1:1) at -70° C., and the mixture was stirred at that temperature for 2 hours, and then at room temperature for one hour. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride, and extracted with diethyl ether. The extract was washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of cyclohexane and ethyl acetate (2:1) as eluent to give 0.27 g of the title compound having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427682
Source datasetuspto-grants-1984_01
ORD IDord-4f0835d2082d400bb8604b3dae8f1693
Source noteuspto-grants-1984_01