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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745852Generated: October 30, 2026

Ethyl 3-chloro-3-oxopropionate → 6-Chloro-1-(4-methoxy-benzyl)-4-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1745852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
ReactantSodium ethoxideHCID 2723922—
Reactant1-[5-Chloro-2-(4-methoxy-benzylamino)-phenyl]-ethanoneHCID 22226606—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product6-Chloro-1-(4-methoxy-benzyl)-4-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid ethyl esterHCID 2102025083.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2 (0.20 g, 1.18 mmol) in 3 mL of anhydrous benzene was treated with ethyl-3-chloro-3-oxopropionate (165 μL, 0.20 g, 1.30 mmol). The reaction mixture was heated to 80° C. for 1 h. The reaction was allowed to cool to room temperature and was concentrated in vacuo. The resulting oil was dissolved in 3 mL of ethanol, treated with NaOEt (40.0 mg, 0.59 mmol). The suspension was heated to 80° C. for 10 min, allowed to cool to room temperature, and diluted with H2O. The resulting white precipitate was filtered to give 3 (0.38 g, 80%) as a white solid. 1H NMR (CDCl3, 400 MHz) δ 7.69 (d, J=2.3 Hz, 1H), 7.39 (dd, J=2.3, 9 Hz, 1H), 7.26 (d, J=9 Hz, 1H), 7.15 (d, J=8.6 Hz, 2H), 6.81 (d, j=8.6 Hz, 2H), 5.47 (br S, 2H), 4.46 (q, J=7.2 Hz, 2H), 3.75 (s, 3H), 2.46 (s, 3H), 1.43 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019141B2
Source datasetuspto-grants-2006_03
ORD IDord-c0049d8151ab4f01931eaebcd1a05a6e
Source noteuspto-grants-2006_03