Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8564Generated: October 23, 2026

Acetic Acid → 1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-one

https://huagongshe.com/en/reaction/8564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetaldehydeHCID 177—
ReactantWaterHCID 962—
Reactant1-(2,6,6-Trimethyl-3-cyclohexen-1-yl)-2-ethanoneHCID 21983366—
SolventButyl AcetateHCID 31272—
Product1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-oneHCID 42296—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a 250 ml flask were added 30 g (0.18 mole) of 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-2-ethanone (94% purity), 12.0 g of butyl acetate, an aliquot according to Table 1 of the catalytic solution as prepared above and a quantity of co-ingredient according to Table 1. The resulting mixture was stirred at 100° C. To said mixture, 4.0 g (0.09 mole) of acetaldehyde, diluted in 10 g of butyl acetate were introduced under the surface of the liquid, over 3 hours. After the completion of the introduction the reaction was cooled to 35° C. To the cooled reaction medium were added 10 g of acetic acid and then 40 ml of water. After stirring a few minutes, the water phase was removed and the organic phase was neutralized by washing it with 25 g of 20% aqueous potassium carbonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091151B2
Source datasetuspto-grants-2006_08
ORD IDord-abb76655ac01447ea0ff9d306d69fe0b
Source noteuspto-grants-2006_08