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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108943Generated: October 30, 2026

Ethyl 2-chloropropionate → Propanoic acid, 2-[4-[(3,5-dichloro-2-pyridinyl)oxy]phenoxy]-, ethyl ester

https://huagongshe.com/reaction/1108943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3,5-Dichloro-pyridin-2-yloxy)-phenolHCID 620880—
ReactantToluene heptaneHCID 22263336—
Catalyst18-Crown-6HCID 28557—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductPropanoic acid, 2-[4-[(3,5-dichloro-2-pyridinyl)oxy]phenoxy]-, ethyl esterHCID 282985564.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

Potassium carbonate (867 g, 6.29 mol) is added to a mixture of p-[(3,5-dichloro-2-pyridyl)oxy]phenol (1,609 g, 6.29 mol), 18-crown-6 (50 g, 0.19 mol) and tetrabutylammonium hydrogen sulfate (50 g, 0.15 mol) in dimethylformamide (20 L). Ethyl 2-chloropropionate (1,380 g, 10.10 mol) is then added and the reaction mixture is stirred for 2 days at 85° C., diluted with water and extracted with methylene chloride. The combined organic extracts are washed sequentially with water, 2% sodium hydroxide solution and water and concentrated in vacuo to give a residue. The residue is dissolved into a 1:1 toluene/heptane solution, washed with 2% sodium hydroxide solution and concentrated in vacuo to obtain the title product as a dark red-brown liquid (1,445 g) which is identified by 1HNMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05318946
Source datasetuspto-grants-1994_06
ORD IDord-23f5e19c43364d0b9c4ea09a4368ffd9
Source noteuspto-grants-1994_06