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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729605Generated: November 2, 2026

Sulfuric Acid → HCID 73794511, compound

https://huagongshe.com/reaction/1729605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,2-DimethylhydrazineHCID 1322—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantHCID 12782786HCID 12782786—
Reactant1-Fluoro-2-nitrosobenzeneHCID 13580904—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 73794511HCID 73794511—

Reaction Steps

A solution of 14.1 g. of o-fluoronitrobenzene in 175 ml. of ethanol and 25 ml. of dimethyl sulfoxide was hydrogenated using 350 mg. of platinum oxide until two equivalents of hydrogen were taken up. The solution of o-fluorophenylhydroxylamine was poured into a solution of 32.5 g. of ferric chloride in 500 ml. of water containing 18 ml. of sulfuric acid at 0°C. After being stirred for 30 minutes, the mixture was shaken with ether and the water was separated. The etheral solution was dried and concentrated to give 10.0 g. of crude o-fluoronitrosobenzene. This was dissolved in 250 ml. of ethyl acetate, cooled to 0°C., and 35.0 g. of mercuric oxide was added. Then 4.8 g. of dimethylhydrazine in 50 ml. of ethyl acetate was added in a dropwise fashion. The mixture was stirred 16 hours at 25°C. and was then filtered through infusorial earth. The filtrate was concentrated and chromatographed on 300 ml of silica in benzene. The product was eluted with ethyl acetate in benzene. One and seven tenths grams of 3,3-dimethyl-1-(o-fluorophenyl)triazene-1-oxide was obtained as a brown oil which gave a satisfactory n.m.r. spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989680
Source datasetuspto-grants-1976_11
ORD IDord-f1590bef81d44cf781d1a9256aa9bdc8
Source noteuspto-grants-1976_11