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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451544Generated: October 30, 2026

1-Naphthaldehyde → 2-Nitro-1-(2-methoxy-1-naphthyl)propene

https://huagongshe.com/reaction/1451544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantNitroethaneHCID 6587—
ReactantAmmonium AcetateHCID 517165—
Product2-Nitro-1-(2-methoxy-1-naphthyl)propeneHCID 5423156095%

Reaction Steps

2.13 g (11.20×10-3 mol) of naphthaldehyde, 30 cm3 of nitroethane and 0.54 g (7×10-3 mol) of ammonium acetate are introduced into a round-bottomed flask. The mixture is stirred and heated to reflux for 2 hours. The nitroethane is then evaporated off under reduced pressure, the residue is taken up with CH2Cl2 and water is added to hydrolyze the acetate. After separation of the two phases, the organic phase is washed with water, the aqueous phases with CH2Cl2 (twice). The organic phase is then dried over MgSO4 and concentrated under reduced pressure. 2.59 g (10.64×10-3 mol) of the expected nitroethylenic compound (yellow solid) are then contained, equivalent to a 95% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604261
Source datasetuspto-grants-1997_02
ORD IDord-260ccd7c489d42e4b0d8a11267147a18
Source noteuspto-grants-1997_02