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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437005Generated: October 28, 2026

Hydrogen Peroxide → 1-Nitroso-3-methylcyclohexane

https://huagongshe.com/reaction/437005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPeracetic AcidHCID 6585—
ReactantAcetic AnhydrideHCID 7918—
Reactant3-Methylcyclohexylamine, mixed isomersHCID 110931—
CatalystSulfuric AcidHCID 1118—
SolventDichloromethaneHCID 6344—
Product1-Nitroso-3-methylcyclohexaneHCID 5395707119.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04029505
Source datasetuspto-grants-1977_06
ORD IDord-15b2486667124edb87a0a317a9c3df9e
Source noteuspto-grants-1977_06