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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645183Generated: October 30, 2026

Ethyl Acetate → HCID 66775565, compound

https://huagongshe.com/reaction/1645183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantPicolyl chloride hydrochlorideHCID 23392—
ReactantMethyl indole-6-carboxylateHCID 639844—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 66775565HCID 66775565—

Reaction Steps

Under a nitrogen atmosphere: to a solution of 1H-indole-6-carboxylic acid methyl ester (for synthesis see example 2a), 2.47 g, 14.1 mmol) in NMP (140 mL) was added Cs2CO3 (10.1 mg, 31 mmol) at 0° C. After stirring for 15 min 2-picolyl chloride hydrochloride (2.77 g, 16.9 mmol) was added and the mixture was stirred at room temperature for 18 h. Ethyl acetate (200 mL) was added and the mixture was washed with saturated aqueous ammonium chloride (3×150 mL) and brine (200 mL). The organic phase was dried (Na2SO4) and concentrated. The crude product was purified using column chromatography (ethyl acetate/heptane 1:3) to give the title compound as a colourless oil, which slowly crystallised on standing (2.72 g, 10.2 mmol, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124647B2
Source datasetuspto-grants-2012_02
ORD IDord-b9eb1fd8c7b243db9c185f56789ef60b
Source noteuspto-grants-2012_02