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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886443Generated: November 2, 2026

Acrylic Acid → 4(1H)-Quinolinone, 8-amino-2,3-dihydro-

https://huagongshe.com/reaction/1886443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
Reactant3-(4-Chloro-2-nitroanilino)propanoic acidHCID 304733—
Reactant3-[(2-Nitrophenyl)amino]propanoic acidHCID 3090203—
Reactant7-chloro-2,3-dihydro-8-nitro-4(1H)-quinolinoneHCID 10727978—
Reactant8-Nitro-2,3-dihydroquinolin-4(1H)-oneHCID 12297362—
Reactant6-fluoro-2,3-dihydro-8-nitro-4(1H)-quinolinoneHCID 18548676—
Reactant3-(3-Chloro-2-nitrophenylamino)propionic acidHCID 19875999—
Reactant2,3-dihydro-7-methyl-8-nitro-4(1H)-quinolinoneHCID 19876009—
ReactantTin hydrochlorideHCID 86739978—
ReactantTin chloride hydrochloric acidHCID 86746162—
CatalystEisenazetatHCID 45051903—
CatalystHydrochloric acid-ironHCID 86633186—
Product4(1H)-Quinolinone, 8-amino-2,3-dihydro-HCID 12297366—

Reaction Steps

By Friedel-Crafts reaction, known compounds 3-(2nitrophenylamino)propionic acid, 3-(4-chloro-2-nitrophenylamino)propionic acid, 3-(3-chloro-2-nitrophenylamino)propionic acid [Ann. Chim. (Rome), volume 55, page 182 (1965)] or substituted N-(2-carboxyethyl)-2-nitroanilin compounds, which can generally be prepared by reacting known substituted 2-nitroaniline with acrylic acid, are converted into novel 2,3-dihydro-8-nitro-4(1H)-quinolinone compounds such as 7-chloro-2,3-dihydro-8-nitro-4(1H)-quinolinone, 6-fluoro-2,3-dihydro-8-nitro-4(1H)-quinolinone and 2,3-dihydro-7-methyl-8-nitro-4(1H)-quinolinone. The 2,3-dihydro-8-nitro-4(1H)-quinolinone compounds are reduced by tin chloride - hydrochloric acid, tin - hydrochloric acid, iron - hydrochloric acid, iron - acetic acid or by catalytic hydrogenation to give 8-amino-2,3-dihydro-4(1H)-quinolinone compounds represented by the formula (IV): ##STR4## wherein R2, R3 and R4 have the same significances as defined above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151431
Source datasetuspto-grants-1992_09
ORD IDord-272a0f32744f437d9d5833e18851c1aa
Source noteuspto-grants-1992_09