Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,2-Dimethylhydrazine | HCID 1322 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | HCID 12782786 | HCID 12782786 | — |
| Reactant | 1-Fluoro-2-nitrosobenzene | HCID 13580904 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 73794511 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03989680 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-f1590bef81d44cf781d1a9256aa9bdc8 |
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| Source note | uspto-grants-1976_11 |
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