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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289164Generated: October 30, 2026

Allyl bromide → 2-Allyl-3-(3-fluoro-phenyl)-pentanedioic acid 1-methyl ester

https://huagongshe.com/reaction/2289164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantLithium diisopropylamideHCID 2724682—
Reactant3-(3-Fluorophenyl)-5-methoxy-5-oxopentanoic acidHCID 45358900—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product2-Allyl-3-(3-fluoro-phenyl)-pentanedioic acid 1-methyl esterHCID 54468642—

Reaction Steps

To a cooled (-78° C.) solution of LDA (7.1 mL, 2.0 M, 14.2 mmol) in 50 mL THF was added a solution of 3-(3-fluoro-phenyl)-pentanedioic acid monomethyl ester (2-4) (1.58 g, 6.58 mmol) in 10 mL THF gradually. The mixture was stirred for 40 min, treated with allyl bromide (1.71 mL, 19.7 mmol) at -78° C. and stirred overnight while it was warmed to room temperature. It was then concentrated and diluted with 20 mL CH2Cl2 and 15 mL EtOH. To the resulting solution was added EDAC (1.88 g, 9.87 mmol) and DMAP (25 mg, 0.02 mmol). After stirring for 5 hr, the reaction was quenched with 20 mL 10% NaHCO3 and extracted with EtOAc (×3). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated to provide 2-5 as an oil, which was further purified using flash silica chromatography (Hexane/EtOAc, 4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090944
Source datasetuspto-grants-2000_07
ORD IDord-890de63308e34afea63bde5429652563
Source noteuspto-grants-2000_07