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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155053Generated: October 30, 2026

3-Chloroaniline → HCID 178522043, compound

https://huagongshe.com/reaction/1155053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanilineHCID 7932—
ReactantTriethylamineHCID 8471—
ReactantHCID 178521117HCID 178521117—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 178522043HCID 17852204354.6%

Reaction Steps

A solution of 4.083 g of m-chloroaniline, 9.71 g of triethylamine and 65 ml of ethyl acetate was poured over 15 minutes at 8° C.-10° C. into a solution of 11.96 g of 2,8-bis-(trifluoromethyl)-4-hydroxy-3-quinoline-carboxylic acid chloride in 130 ml of ethyl acetate with violent stirring and the temperature was allowed to return to room temperature. The mixture was refluxed for one hour and was cooled and vacuum filtered. The filtrate was washed with water, was dried and evaporated to dryness at 40° C. under reduced pressure to obtain 17.14 g of a triethylamine salt. The residue was dissolved in 2 N sodium hydroxide solution which was then heated to reflux and cooled to room temperature. The mixture was vacuum filtered and the recovered product was dissolved in water. The solution was adjusted to a pH of 1 by addition of 20% hydrochloric acid and the mixture was vacuum filtered. The recovered product was crystallized from benzene to obtain 7.599 g of 2,8-bis-(trifluoromethyl)-4-hydroxy-N-(3-chlorophenyl)-3-quinolinecarboxamide melting at 152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04299831
Source datasetuspto-grants-1981_11
ORD IDord-44bfbdf56a5446859e340eb2de5a9678
Source noteuspto-grants-1981_11