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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423358Generated: November 1, 2026

Nitroethane → 1-Nitro-2-(2-nitroprop-1-en-1-yl)benzene

https://huagongshe.com/reaction/1423358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product1-Nitro-2-(2-nitroprop-1-en-1-yl)benzeneHCID 2731316—

Reaction Steps

A solution of 2-nitrobenzaldehyde (5.0 g, 33.1 mmol) and ammonium acetate (2.55 g, 33.1 mmol) in AcOH (20 mL) was treated dropwise at 20° C. with nitroethane (2.84 mL, 39.7 mmol). The resulting solution was heated under reflux for 2 h, then cooled and diluted with EtOAc. The organic layer was washed with saturated aqueous NaHCO3 solution and brine, then dried over Na2SO4. Filtration and removal of the volatiles gave a residue that was purified on silica gel (gradient elution, 0-40% EtOAc/hexanes) to give the title compound as an oil. (2.3 g, 33%). LCMS (ES+) m/z 209 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927569B2
Source datasetuspto-grants-2015_01
ORD IDord-b42400b64d574091ad497799822f2ea2
Source noteuspto-grants-2015_01