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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128773Generated: October 26, 2026

1-Naphthaldehyde → HCID 54231560, compound

https://huagongshe.com/reaction/128773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantNitroethaneHCID 6587—
ReactantAmmonium AcetateHCID 517165—
ProductHCID 54231560HCID 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 obtained, equivalent to a 95% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464872
Source datasetuspto-grants-1995_11
ORD IDord-19fe6cc18fd94628b72c94279e7141f8
Source noteuspto-grants-1995_11