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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716487Generated: October 30, 2026

Cyclohexanone → 1-Oxaspiro[5.5]undec-3-ene, 4-methyl-

https://huagongshe.com/reaction/716487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
Reactant3-Methyl-3-buten-1-olHCID 12988—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product1-Oxaspiro[5.5]undec-3-ene, 4-methyl-HCID 1111642480%

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of p-TSA (20 g, 0.105 mol) and toluene (2 L) was heated to 115° C. To this mixture were added cyclohexanone (980 g, 10 mols) and isoprenol (946 g, 11 mols) and heated further for 3-6 h. Water was removed from the reaction azeotropically. The reaction mixture was then cooled to room temperature. The organic phase was washed with a 5% Na2CO3 solution, washed with water dried and concentrated and distilled further to provide 4-methyl-1-oxaspiro [5.5] undec-3-ene (1.32 kg) having a purity of 98% (sum of the isomers) for a total yield of 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187709B2
Source datasetuspto-grants-2015_11
ORD IDord-164427831c5d4e9e8728c6430438f806
Source noteuspto-grants-2015_11