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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968736Generated: October 26, 2026

Selenious Acid → (7-Chloro-2-formyl-quinolin-8-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/1968736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenious AcidHCID 1091—
Reactant(7-Chloro-2-methyl-quinolin-8-yl)-acetic acid ethyl esterHCID 66882026—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(7-Chloro-2-formyl-quinolin-8-yl)-acetic acid ethyl esterHCID 8625392677%

Reaction Conditions

Temperature100 °C

Reaction Steps

Selenious acid (193 mg, 1.50 mmol, 1.1 equiv) was added to a solution of (7-chloro-2-methyl-quinolin-8-yl)-acetic acid ethyl ester in dioxane (12 ml). The reaction mixture was heated to 100° C. After 20 and 40 minutes, additional portions of selenious acid (88 mg each) were added, and heating was continued for a total of 90 minutes. After cooling, the reaction mixture was diluted with water, filtered, and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified via flash chromatography (gradient of hexane/EtOAc 100:0 to 80:20) to afford the title compound (292 mg, 77%). 1H NMR (400 MHz, CDCl3): δ=10.18 (s, 1H), 8.31 (d, J=8.1 Hz, 1H), 8.04 (d, J=8.1 Hz, 1H), 7.82 (d, J=7.7 Hz, 1H), 7.71 (d, J=7.7 Hz, 1H), 4.61 (s, 2H), 4.22 (q, J=7.3 Hz, 2H), 1.28 (t, J=7.3 Hz, 3H). MS (ES+): 278.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426440B2
Source datasetuspto-grants-2013_04
ORD IDord-58902b319efe4c09be849408d2ceeff7
Source noteuspto-grants-2013_04