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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392352Generated: November 2, 2026

Sulfuric Acid → 4-(4-tert-Butylphenyl)-2-(propan-2-yl)-1H-indene

https://huagongshe.com/reaction/1392352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Isopropyl-7-(4'-tert-butylphenyl)-1-indanoneHCID 23105546—
SolventMethanolHCID 887—
Product4-(4-tert-Butylphenyl)-2-(propan-2-yl)-1H-indeneHCID 1798040596.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

4.83 g of sodium borohydride and 39.1 g of 2-isopropyl-7-(4′-tert-butylphenyl)-1-indanone together with 118 ml of toluene are placed in a reaction vessel. At 50° C., 22.5 ml of methanol are slowly added and the reaction mixture is stirred for 6 hours at 50° C. After cooling to room temperature, 50 ml of 2N sulfuric acid are added and the mixture is stirred vigorously for another 30 minutes. The mixture is subsequently transferred to a separating funnel, the phases are separated and the aqueous phase is shaken twice with a total of 60 ml of 2N sulfuric acid. The organic phases are combined and dried over magnesium sulfate. The solvent of the reaction mixture is removed virtually completely and 200 ml of toluene and 0.4 g of p-toluenesulfonic acid are subsequently added to the residue. Water is distilled from the reaction mixture by heating for 1.5 hours on a water separator until reaction is complete. The reaction mixture is subsequently washed once with 100 ml of saturated sodium hydrogen carbonate solution and dried over magnesium sulfate. After separating off the magnesium sulfate, the residue is dried in an oil pump vacuum. This gives 35.7 g of 2-isopropyl-4-(4′-tert-butylphenyl)indene (total yield: 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342078B2
Source datasetuspto-grants-2008_03
ORD IDord-e5a39ebceb5c41328afe5f714c5d5dc4
Source noteuspto-grants-2008_03