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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518668Generated: November 3, 2026

Ethyl Acetate → HCID 66810209, compound

https://huagongshe.com/reaction/1518668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-Chloroethyl chloroformateHCID 12305—
ReactantSodium hydrideHCID 24758—
ReactantAripiprazoleHCID 60795—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 66810209HCID 66810209—

Reaction Steps

To a suspension of aripiprazole (2.0 g, 4.46 mmol) in 2-methyltetrahydrofuran (50 mL) was added NaH (357 mg, 8.92 mmol). The reaction was stirred overnight at room temperature then chloroethyl chloroformate (1.46 mL, 13.38 mmol) was added. Further 2-methyltetrahydrofuran (10 mL) was added to aid stirring. The reaction was stirred overnight at room temperature. The reaction was cooled to 0° C., diluted with ethyl acetate (50 mL) and quenched with aqueous saturated NaHCO3 (50 mL). The reaction was extracted with ethyl acetate (3×50 mL). The combined organics were dried (MgSO4) and concentrated to give 1-chloroethyl 7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinoline-1(2H)-carboxylate (crude yield 2.22 g) as a 3:2 mixture of aripiprazole/product. The product was taken onto the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09072788B2
Source datasetuspto-grants-2015_07
ORD IDord-2471cc4d3033463f9bbe7b22f568e6d6
Source noteuspto-grants-2015_07