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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542908Generated: October 25, 2026

Sulfuric Acid → (E)-4-(2-(4,5,6,7-Tetrahydro-4,4,7,7-tetramethylbenzo(b)thien-2-yl)-1-propenyl)benzoic acid

https://huagongshe.com/reaction/542908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl p-[2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]-benzoateHCID 53678243—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(E)-4-(2-(4,5,6,7-Tetrahydro-4,4,7,7-tetramethylbenzo(b)thien-2-yl)-1-propenyl)benzoic acidHCID 643976386.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

3.0 g of ethyl p-[2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]benzoate are dissolved in 100 ml of ethanol and the solution is treated with a solution of 3.9 g of potassium hydroxide in 20 ml of water. After stirring at 50° C. for 3 hours, the mixture is cooled, poured into ice-water and acidified with 2N sulphuric acid. The mixture is extracted with ethyl acetate, the organic phase is washed with water, dried over sodium sulphate and evaporated. After recrystalization of the residue from ethyl acetate, there are obtained 2.4 g of p-[(E)-2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]benzoic acid in the form of pale yellowish crystals, m.p. 236°-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659735
Source datasetuspto-grants-1987_04
ORD IDord-e3936f81073c4ac3b9f4e5c38b14f997
Source noteuspto-grants-1987_04