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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474328Generated: October 25, 2026

1,1'-Carbonyldiimidazole → Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/474328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-Chloro-2-methylbenzoic acidHCID 82009—
ReactantPotassium ethyl malonateHCID 3446434—
ReactantMagnesium ChlorideHCID 5360315—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoateHCID 54012347118%

Reaction Steps

To a stirring solution of 5-chloro-2-methylbenzoic acid (4.85 g, 28.4 mmol) in tetrahydrofuran (30 mL) was added N,N-carbonyldiimidazole (4.87 g, 30.0 mmol, 1.06 equiv). After 30 minutes, the reaction mixture was added to a suspension of potassium ethyl malonate (11.61 g, 68.22 mmol, 2.40 equiv) and magnesium chloride (3.27 g, 34.3 mmol, 1.21 equiv) in tetrahydrofuran (50 mL). The resultant suspension was heated at 50° C. After hours, the reaction mixture was partitioned between ethyl acetate and water. The organic portion was dried over magnesium sulfate, filtered, and concentrated to provide 8.07 g (118%) of ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate which was used without purification. LCMS (ESI) m+H=241.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637526B2
Source datasetuspto-grants-2014_01
ORD IDord-6902af7ba6ec4cafb811af10766cae5d
Source noteuspto-grants-2014_01