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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372770Generated: October 31, 2026

Hydrogen Peroxide → HCID 20326677, compound

https://huagongshe.com/reaction/372770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantHCID 20326684HCID 20326684—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 20326677HCID 2032667763%
ProductHCID 20326684HCID 20326684—

Reaction Steps

A solution of peroxytrifluoracetic acid was prepared from 1.70 ml, 0.062 moles, of 90% hydrogen peroxide, 10.5 ml, 0.074 moles, of trifluoroacetic anhydride, and 12 ml of methylene chloride. This reagent was added over a 35 minute period to a well stirred, boiling mixture of 8.2 g, 0.048 moles, of 1,1-dinitro-1-cyano-3-butene, 50 ml of methylene chloride, and 27.5 g, 0.192 moles, of disodium hydrogen phosphate. After this mild exothermic reaction had subsided, the solution was heated under reflux for 21/2 hours. The resulting mixture was stirred with 75 ml of water until all the inorganic salts had dissolved. The organic layer was separated and the aqueous layer was extracted with 2-10 ml portions of methylene chloride. The combined methylene chloride extracts were washed with 15 ml of 10% sodium bicarbonate solution and dried over magnesium sulfate. The solvent was removed at reduced pressure and the residual liquid was fractionated through a small Vigreux column to yield 3.6 g of unreacted 1,1-dinitro-1-cyano-3-butene and 3.17 g (63% yield) of 1,1-dinitro-1-cyano-3,4-epoxybutane, b.p. 62°-64°/0.005 mm., N25D 1.4672. The infrared spectrum was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04092336
Source datasetuspto-grants-1978_05
ORD IDord-27e9e06a13324dceb288672f47150f35
Source noteuspto-grants-1978_05