Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14355Generated: October 26, 2026

Hydrochloric Acid → 4-Hydroxy-1-methyl-3-nitro-1,2-dihydroquinolin-2-one

https://huagongshe.com/reaction/14355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantN-Methylisatoic anhydrideHCID 25160—
ReactantEthyl nitroacetateHCID 69379—
ReactantHCID 178418361HCID 178418361—
SolventDimethylacetamideHCID 31374—
Product4-Hydroxy-1-methyl-3-nitro-1,2-dihydroquinolin-2-oneHCID 5468212327%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of ethylnitroacetate (15.96 g, 120 mmol) was added slowly in a suspension of sodium hydride (60% in mineral oil, 5.28 g, 132 mmol) in dimethylacetamide under N2 atmosphere. The mixture was allowed to stir at room temperature until the evolution of hydrogen gas ceased, then heated to 90° C. for 30 min. and cooled to room temperature. A solution of N-methylisatoic anhydride (23.38 g, 132 mmol) in dimethylacetamide was added slowly and heated overnight at 120° C. The mixture was cooled to room temperature, poured into ice water, and acidified by cold 10% HCl. The solids formed were filtered and washed several times by water to yield 7.1 g (27%) of yellow solids. Mp 193° C. 1H NMR (DMSO-d6): δ 3.60 (s, 3H), 7.37 (t, J=7.6 Hz, 1H), 7.58 (d, J=8.5 Hz, 1H), 7.77 (t, J=7.5 Hz, 1H), 8.12 (d, J=7.9 Hz, 1H). EIMS m/z 221 (M+1), 243 (M+23). Anal. (C10H8N2O4) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732146B2
Source datasetuspto-grants-2010_06
ORD IDord-f5f4df6862dd4fd2a27a8204c0be1017
Source noteuspto-grants-2010_06