HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437005Generated: October 28, 2026
Hydrogen Peroxide → 1-Nitroso-3-methylcyclohexane
https://huagongshe.com/reaction/437005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Methylcyclohexylamine, mixed isomers | HCID 110931 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Nitroso-3-methylcyclohexane | HCID 53957071 | 19.5% |
Reaction Steps
1-Nitroso-3-methylcyclohexane dimer was prepared as follows: Acetic anhydride (55 g) was added over a 30-minute period, to a solution of 12.2 ml of 90% hydrogen peroxide and one drop of concentrated sulfuric acid in 50 ml of methylene chloride, while the temperature was maintained at 0° C. This solution was then added slowly to 22.8 g of 3-methylcyclohexylamine in 75 ml of methylene chloride while the temperature was maintained at 15° C. After the addition of the peracetic acid solution was completed, the reaction mixture was allowed to warm to room temperature and stirred an additional 10 hours. The solution was extracted with 200 ml of water, 100 ml of cold 15% ammonium hydroxide, 100 ml of 10% sulfuric acid and 100 ml of water, and dried over anhydrous magnesium sulfate. The methylene chloride was removed by distillation to leave a pale blue solid. This solid was recrystallized from methanol-water to give 5.0 g of 1 -nitroso-3-methylcyclohexane dimer as a white solid, mp 81°-83° C. The structure was confirmed by IR, UV and NMR spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04029505 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-15b2486667124edb87a0a317a9c3df9e |
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| Source note | uspto-grants-1977_06 |
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