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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52543Generated: October 30, 2026

2-Ethoxalylmethylcarbonylquinoline → 1-(Quinolin-2-yl)ethan-1-one

https://huagongshe.com/reaction/52543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthoxalylmethylcarbonylquinolineHCID 19963236—
SolventHydrochloric AcidHCID 313—
Product1-(Quinolin-2-yl)ethan-1-oneHCID 31870396.1%

Reaction Steps

A solution of 2-ethoxalylmethylcarbonylquinoline (32.24 g, 0.132 mol) in concentrated hydrochloric acid (300 mL) was refluxed for 4 h and concentrated in vacuo. The residue was dissolved in aqueous sodium bicarbonate and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography with 20:1 to 7:1 hexane/ethyl acetate to give 21.72 g of 2-acetylquinoline (96%): 1H NMR (270 MHz, CDCl3) δ8.25 (d, 1H, J=8.6 Hz), 8.19 (dd, 1H, J=8.3, 1 Hz), 8.13 (d, 1H, J=8.6 Hz), 7.86 (dd, 1H, J=8.3, 1 Hz), 7.78 (td, 1H, J=8.3, 1 Hz), 7.64 (td, 1H, J=8.3, 1 Hz), 2.87 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616586
Source datasetuspto-grants-1997_04
ORD IDord-d2d9c123015b44638b752ce959daefa7
Source noteuspto-grants-1997_04