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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987204Generated: October 30, 2026

Water → 2'-Nitrobenzanilide

https://huagongshe.com/reaction/987204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-NitroanilineHCID 6946—
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product2'-NitrobenzanilideHCID 69769—

Reaction Steps

1.58 g of sodium hydride (60% content) was suspended in 19.80 g of tetrahydrofuran and cooled with ice. To the obtained suspension, 19.83 g of a tetrahydrofuran solution containing 2.50 g of 2-nitroaniline was dropwise added over 1 hour, stirred for 10 minutes, allowed to stand at room temperature and stirred for 30 minutes. To the obtained mixture, 2.77 g of benzoyl chloride was added dropwise over 0.5 hr at room temperature and stirred for 2 hours. The reaction mixture was added to water and separated. The separated organic layer was washed with sodium hydroxide solution and saline to obtain an organic layer, which was analyzed by high performance liquid chromatography to find the yield of the desired product was 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630598B2
Source datasetuspto-grants-2003_10
ORD IDord-1092eb530ff34927945f1dc89734a848
Source noteuspto-grants-2003_10