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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427013Generated: October 27, 2026

Nitromethane → (E)-2-(Benzyloxy)-1-ethoxy-4-(2-nitrovinyl)benzene

https://huagongshe.com/reaction/1427013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant3-(Benzyloxy)-4-ethoxybenzaldehydeHCID 818573—
SolventAcetic AcidHCID 176—
Product(E)-2-(Benzyloxy)-1-ethoxy-4-(2-nitrovinyl)benzeneHCID 86730317—

Reaction Conditions

Temperature130 °C

Reaction Steps

3-(Benzyloxy)-4-ethoxy benzaldehyde described in Production Example 15-2 (14.5 g, 56.4 mmol) was dissolved in acetic acid (45 mL), then ammonium acetate (5.22 g, 67.7 mmol) and nitromethane (7.5 mL, 138 mmol) were added under nitrogen atmosphere at room temperature, and the mixture was heated and stirred at 130° C. for 2.5 hours. The mixture was cooled to room temperature and the precipitate was collected by filteration and washed with ethanol to quantitatively obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933099B2
Source datasetuspto-grants-2015_01
ORD IDord-14da2fb00edb4a4eb7b54a86918448d5
Source noteuspto-grants-2015_01