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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892673Generated: October 30, 2026

Acetone → HCID 22844417, compound

https://huagongshe.com/reaction/892673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl vinyl ketoneHCID 6570—
ReactantHCID 57294670HCID 57294670—
ReactantHCID 178418582HCID 178418582—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 22844417HCID 22844417—

Reaction Steps

This compound was prepared by aldol condensation of 2 g (0.011 mol) of (+)-(1R,5S)-5-ethyl-2,6,6-trimethyl-2-cyclohexen-1-carbaldehyde (obtained according to example 4i.) with 2 ml (0.03 mol) of acetone, in 10 ml of ethanol. After adding 0.1 ml of a 30% solution of CH3ONa in methanol, the reaction was allowed to proceed for about 65 h. Following the usual treatment, 1.3 g of 95% pure mixture were obtained, containing 83% of the above-mentioned butenone, 13% of its α-trans isomer and 4% of its α-cis isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118865
Source datasetuspto-grants-1992_06
ORD IDord-78b2726e3119468884b95930392f9853
Source noteuspto-grants-1992_06