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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272539Generated: October 30, 2026

Nitromethane → 5-(2-Nitroethenyl)-1,3-benzodioxole

https://huagongshe.com/reaction/1272539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantPiperonalHCID 8438—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
Product5-(2-Nitroethenyl)-1,3-benzodioxoleHCID 9494580%

Reaction Conditions

Temperature70 °C

Reaction Steps

To piperonal (15.55 kg, 103.5 mol) under mechanical stirring and under nitrogen was added ammonium acetate (13.4 kg, 173.8 mol), acetic acid (45.2 kg), and nitromethane (18.4 kg, 301.4 mol) sequentially. The mixture was warmed to 70° C. After about 30 minutes, the yellow product began to crystallize. The reaction temperature was raised to 80° C. and stirred for about 10 hours until minimal piperonal remains. The somewhat thick reaction mixture was cooled to 10° C. and filtered. The precipitate was washed with acetic acid (2×8 kg) and then water (2×90 kg). The product was dried under a nitrogen purge and then in a vacuum oven at 50° C. for 2 days to afford 15.94 kg (80%) of the title compound as a bright yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208517B1
Source datasetuspto-grants-2007_04
ORD IDord-d95b87242ea84599a3487ba9f694b72f
Source noteuspto-grants-2007_04