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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444382Generated: October 30, 2026

1-(3,3,5-Trimethyl-1-cyclohexen-1-yl)pent-4-en-1-one → 1-(3,3,4-Trimethyl-cyclohex-6-en-1-yl)-pent-4-en-1-one

https://huagongshe.com/reaction/444382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3,3,5-Trimethyl-1-cyclohexen-1-yl)pent-4-en-1-oneHCID 92608—
Reactant1-Ethynyl-3,3,5-trimethylcyclohexanolHCID 233268—
Product1-(3,3,4-Trimethyl-cyclohex-6-en-1-yl)-pent-4-en-1-oneHCID 20569424—

Reaction Steps

1-Hydroxy-1-ethynyl-3,3,5-trimethyl-cyclohexane used as starting material for the following preparation was prepared in accordance with W. Ziegenstein, "Aethinylierung und Alkinylierung", p. 9, Verlag Chemie (1963). The conversion into 1-(3,3,5-trimethyl-cyclohex-1-en-1-yl)-pent-4-en-1-one was performed according to the procedure described in pathway I, paragraph (d). The analytical data were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264467
Source datasetuspto-grants-1981_04
ORD IDord-3e4c0672461f44c39e07a3e8e8e20a85
Source noteuspto-grants-1981_04