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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350131Generated: October 26, 2026

Ethyl 4,4,4-trifluoroacetoacetate → 5-amino-7-chloro-3,4-dihydro-4-hydroxy-4-(trifluoromethyl)-1H-quinolin-2-one

https://huagongshe.com/reaction/1350131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
Reactant1,3-Benzenediamine, 5-chloro-HCID 73335—
SolventEthanolHCID 702—
Product5-amino-7-chloro-3,4-dihydro-4-hydroxy-4-(trifluoromethyl)-1H-quinolin-2-oneHCID 2227917937%

Reaction Steps

To a solution of 5-chloro-1,3-phenylenediamine (15.0 g, 0.105 mol) in 70 mL ethanol was added ethyl 4,4,4-trifluoroacetoacetate (20.4 g, 0.111 mol), then the mixture was heated at reflux for 18 h. The solvent was removed under reduced pressure until the product began to precipitate. The material was allowed to crystallize for 2 h, whereupon it was filtered and rinsed with cold ether to afford 10.9 g (37%) of 5-amino-7-chloro-3,4-dihydro-4-hydroxy-4-(trifluoromethyl)-1H-quinolin-2-one, a tan solid. The filtrate was concentrated until solid began to precipitate and afforded an additional 3.0 g (10%). 1H NMR (400 MHz, acetone-d6) δ 11.0 (broad s, 1H), 9.64 (s, 1H), 7.42 (t, 1H, J=8.1), 6.99 (d, 1H, J=8.1), 6.90 (s, 1H), 6.79 (d, 1H, J=8.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214690B2
Source datasetuspto-grants-2007_05
ORD IDord-34d282bd727d45d7bb7205cb97055b8a
Source noteuspto-grants-2007_05