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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243411Generated: November 3, 2026

Isatoic Anhydride → HCID 58601126, compound

https://huagongshe.com/reaction/2243411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsatoic AnhydrideHCID 8359—
ReactantBenzenepropanoic acid, 4-nitro-beta-oxo-, ethyl esterHCID 13281—
ReactantSodium hydrideHCID 24758—
SolventDimethylacetamideHCID 31374—
ProductHCID 58601126HCID 5860112628%

Reaction Conditions

Temperature120 °C

Reaction Steps

Sodium hydride (0.92 g, 0.023 mol; 60% suspension in mineral oil) was added portionwise to a stirred solution of 3-(4-nitrophenyl)-3-oxopropionic acid ethyl ester (5.46 g, 0.023 mol) in dimethylacetamide (20 mL) at room temperature. A solution of isatoic anhydride (3.4 g, 0.02 mol) in dimethylacetamide (20 mL) was added to this solution. The reddish mixture was stirred at 120° C. for 30 min and then the solvent was concentrated in vacuo. The crude solid was partitioned between water and ethyl acetate and the organic phase then separated. The combined organic extracts were dried over sodium sulfate and concentrated in vacuo to leave a residue which was washed once with cold tert-butylmethyl ether to yield 2-(4-nitrophenyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester (1.61 g, 28%) as a white solid, LCMS m/z 339.33 [M+H]+ @ RT 1.16 min, 100% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674906B2
Source datasetuspto-grants-2010_03
ORD IDord-9b86c2265d2b4385a6d2a5b716b6a965
Source noteuspto-grants-2010_03