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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116547Generated: October 26, 2026

Water → N-ethyl 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide

https://huagongshe.com/reaction/2116547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Hydroxy-5-chloropyridineHCID 582305—
ReactantN-ethyl-2-chloro-5-nitrobenzamideHCID 4380195—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-ethyl 5-nitro-2-(3-chloro-5-pyridyloxy)benzamideHCID 1210936252%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of potassium t-butoxide (1.5 g) in THF (15 mL) was added 3-chloro-5-hydroxypyridine (1.79 g, mmol). To this solution was added a solution of N-ethyl-2-chloro-5-nitrobenzamide (2.76 g, mmol) in THF (15 mL). The resulting mixture was heated at 50° C. for 84 hr. After cooling, the reaction mixture was diluted into a mixture of water and ether. Solids were collected by filtration, washed with water then with ether, and dried under vacuum to afford N-ethyl 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide (2.0 g, 52%). mp 165-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439242B2
Source datasetuspto-grants-2008_10
ORD IDord-2bc463a7060b4a2c8b2bb2cf071ed580
Source noteuspto-grants-2008_10