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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758150Generated: October 31, 2026

Ethylene Glycol → Trans-3-[2-Benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-(2-propenyl)cyclohexanone ethylene ketal

https://huagongshe.com/reaction/1758150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantSodium HydroxideHCID 14798—
ReactantTrans-3-[2-Benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-(2-propenyl)cyclohexanoneHCID 13105165—
ReactantHCID 178427284HCID 178427284—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductTrans-3-[2-Benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-(2-propenyl)cyclohexanone ethylene ketalHCID 86738780—

Reaction Steps

A mixture of 17.0 g. (38.1 mmoles) of trans-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-(2-propenyl)cyclohexanone, 47.2 g. (0.762 mole) ethylene glycol and 250 mg. of p-toluenesulfonic acid monohydride in 200 ml. of benzene was heated at reflux for 3 hours with a Dean-Stark trap. The reaction was cooled and added to 200 ml. 1 N sodium hydroxide, 100 ml. ether and 100 ml. pentane. The organic extract was washed twice with 200 ml. portions of water, twice with 200 ml. portions of saturated sodium chloride, dried over magnesium sulfate and evaporated (aspirator) giving a quantitative yield of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371720
Source datasetuspto-grants-1983_02
ORD IDord-ab64f69e983c44b3a8ad03387608efe0
Source noteuspto-grants-1983_02