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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550349Generated: October 30, 2026

Water → N-(3,4-dichlorophenyl)-3-nitro-2-piperid-1-yl-5-trifluoromethylbenzamide

https://huagongshe.com/reaction/550349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
ReactantN-(3,4-dichlorophenyl)-2-chloro-3-nitro-5-trifluoromethylbenzamideHCID 86620253—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Solvent1,4-DioxaneHCID 31275—
ProductN-(3,4-dichlorophenyl)-3-nitro-2-piperid-1-yl-5-trifluoromethylbenzamideHCID 11854386—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of N-(3,4-dichlorophenyl)-2-chloro-3-nitro-5-trifluoromethylbenzamide (0.76 g; 1 eq.) in dioxane (12 ml) is added piperidine (0.4 ml; 2.2 eq.). After stirring for 18 hours at 25° C., 10 ml of water are added and the product is extracted with ethyl acetate. The organic phase is dried and concentrated. The orange oil obtained is dissolved in 2 ml of ethyl ether and 120 ml of hexane. After 3 days at 0° C., the solid is filtered off by suction and dried. 540 mg of N-(3,4-dichlorophenyl)-3-nitro-2-piperid-1-yl-5-trifluoromethylbenzamide are obtained (m.p.=144° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947675B2
Source datasetuspto-grants-2011_05
ORD IDord-7348f71b401b49b7b8cf85ea219973b1
Source noteuspto-grants-2011_05