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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905352Generated: October 26, 2026

Sulfuric Acid → 6-Isopropyl-2-methyl-3-cyclohexene-1-carboxylic acid

https://huagongshe.com/reaction/1905352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPenta-1,3-dieneHCID 15301—
Reactant4-Methyl-pent-2-enoic acidHCID 112103—
Reactant3-Isopropyl acrylic acidHCID 642039—
SolventDiethyl EtherHCID 3283—
Product6-Isopropyl-2-methyl-3-cyclohexene-1-carboxylic acidHCID 2003541265.7%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 70 g (0.61 mol) of trans-4-methyl-2-pentenoic acid and 49 g (0.72 mol) of 1,3-pentadiene was heated for 12 hours at approx. 200° C. in an autoclave. After the reaction mixture had cooled, it was checked by means of GLC for the presence of 4-methyl-2-pentenoic acid. A further 25 g (0.36 mol) of 1,3-pentadiene were added, after which the mixture was again heated for 12 hours at 200° C. This procedure was repeated until no further decrease in the content of 4-methyl-2-pentenoic acid was any longer observed. The reaction mixture obtained was dissolved in 300 ml of ether and extracted with 300 ml of 10% NaOH solution. The alkaline solution thus obtained was acidified with 40 g of concentrated sulphuric acid and then extracted three times with ether. The ether extract was washed with water, dried on MgSO4, evaporated down and distilled. 73 g of 6-isopropyl-2-methyl-3-cyclohexene-1-carboxylic acid were obtained, b.p.: 95°-100° C./70 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843061
Source datasetuspto-grants-1989_06
ORD IDord-34827857b5414388885e7bf4867918d7
Source noteuspto-grants-1989_06