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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543431Generated: November 1, 2026

Nitroethane → 1-Methoxy-3-(2-nitroprop-1-enyl)benzene

https://huagongshe.com/reaction/543431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
Reactant3-MethoxybenzaldehydeHCID 11569—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
Product1-Methoxy-3-(2-nitroprop-1-enyl)benzeneHCID 606259—

Reaction Steps

A mixture of 71.9 g (0.528 mole) of m-anisaldehyde, 118.9 g (1.584 mole) of nitroethane, 40.7 g (0.528 mole) of ammonium acetate, and 350 ml of glacial acetic acid was heated to reflux for one hour. The mixture was then allowed to cool and partitioned between ether and water. The ether layer was separated and washed sequentially with water, 3N sodium hydroxide, water and brine. The organic phase was dried over anhydrous magnesium sulfate and evaporated in vacuo to give the crude product. After a preliminary distillation at 125° C./0.0001 mm, the product was finally crystallized from absolute ethanol to yield the pure product, a yellow solid, mp 40°-42° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661635
Source datasetuspto-grants-1987_04
ORD IDord-0725bd92c2eb4247ac379984af9d2ce7
Source noteuspto-grants-1987_04