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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106093Generated: October 26, 2026

Sulfuric Acid → 3-(3-Oxobut-1-enyl)-2,4,4-trimethylcyclohex-2-en-1-one

https://huagongshe.com/reaction/1106093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium dichromate dihydrateHCID 108005—
Reactant4-(3-Hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-oneHCID 54034727—
SolventDiethyl EtherHCID 3283—
Product3-(3-Oxobut-1-enyl)-2,4,4-trimethylcyclohex-2-en-1-oneHCID 33736734.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution, pre-cooled to 0° C., of 140 g (0.068 mol) of 4-(2,6,6-trimethyl-3-hydroxy-cyclohex-1-en-1-yl)-but-3-en-2-one in 500 ml of ether are added dropwise over a period of 10 minutes 700 ml of an aqueous solution, cooled to 0° C., of 202.6 g of sodium dichromate dihydrate and 186 g of concentrated sulphuric acid with intensive cooling and good stirring so that a temperature of 5° C. is not exceeded. The mixture is then stirred for a further 5 minutes at 5° C., treated with 500 ml of ether, the ether phase is washed three times with water, three times with soda solution and again three times with water, dried over sodium sulphate and concentrated. Distillation of the resulting 125 g of crude product over a 10 cm Widmer column gave 103 g of more than 94% pure 4-(2,6,6-trimethyl-3-oxo-cyclohex-1-en-1-yl)-but- 3-en-2-one of boiling point 109°-110° C./0.05 mm Hg; melting point 50°-51° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04311718
Source datasetuspto-grants-1982_01
ORD IDord-f6f2645b82d4426cbf7dd5593ee9b3f5
Source noteuspto-grants-1982_01