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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241225Generated: October 31, 2026

Nitric Acid → 1-(6-Nitro-1,3-benzodioxol-5-yl)ethan-1-one

https://huagongshe.com/reaction/1241225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantEthyl AcetateHCID 8857—
ReactantAcetopiperoneHCID 76622—
SolventAcetic AcidHCID 176—
SolventHexaneHCID 8058—
Product1-(6-Nitro-1,3-benzodioxol-5-yl)ethan-1-oneHCID 92022—

Reaction Steps

A solution of 50 g (0.305 mole) 3,4-methylenedioxy-acetophenone (Aldrich) in 200 mL glacial acetic acid was added dropwise over 30 minutes to 700 mL of cold (2–4° C.) 70% HNO3 with stirring (NOTE: the reaction will overheat without external cooling from an ice bath, which can be dangerous and lead to side products). At temperatures below 0° C., however, the reaction can be sluggish. A temperature of 3–5° C. seems to be optimal). The mixture was left stirring for another 60 minutes at 3–5° C., and then allowed to approach ambient temperature. Analysis by TLC (25% EtOAc in hexane) indicated complete conversion of the starting material within 1–2 hr. When the reaction was complete, the mixture was poured into ˜3 liters of crushed ice, and the resulting yellow solid was filtered off, washed with water and then suction-dried. Yield 53 g (84%), used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115364B1
Source datasetuspto-grants-2006_10
ORD IDord-60c5e1bbaeb54e9ab91ffdc73e33254f
Source noteuspto-grants-2006_10