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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658235Generated: November 1, 2026

Nitric Acid → 5,7-Dihydro-5,5,7,7-tetramethyl-3-(3-nitrophenyl)furo(3,4-e)-as-triazine 4-oxide

https://huagongshe.com/reaction/1658235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantSodium BicarbonateHCID 516892—
Reactant5,5,7,7-tetramethyl-4-oxido-3-phenylfuro[3,4-e][1,2,4]triazin-4-iumHCID 6412720—
SolventDichloromethaneHCID 6344—
Product5,7-Dihydro-5,5,7,7-tetramethyl-3-(3-nitrophenyl)furo(3,4-e)-as-triazine 4-oxideHCID 72729—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a mixture of 0.2 ml (0.005 mole) of fuming nitric acid and 1.5 grams (0.01 mole) of trifluoromethanesulfonic acid in 15 ml. anhydrous methylene chloride, after allowing the resulting mixture to be stirred for 1 hour at 25°C., there is added dropwise maintaining the temperature at -30°C., 0.542 grams (0.002 mole) of 5,7-dihydro-5,5,7,7-tetramethyl-3-phenylfuro [3,4-e]-as-triazine-4-oxide in 15 ml. of anhydrous methylene chloride. The resulting heterogeneous mixture is stirred at 25°C. for 72 hours, poured onto ice, and neutralized with solid sodium bicarbonate. The organic layer is removed and the aqueous phase extracted several times with methylene chloride. The combined organic layers are washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and evaporated to give a white solid. The resulting solid is recrystallized from methylene chloride/hexane to give 5,7-dihydro-5,5,7,7-tetramethyl-3-(m-nitrophenyl)-furo[3,4-e]-as-triazine-4-oxide, m.p. 202°-204°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963713
Source datasetuspto-grants-1976_06
ORD IDord-c4deb43b7169493586ed606372f41474
Source noteuspto-grants-1976_06