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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54865Generated: October 28, 2026

Phthalic Anhydride → 2-(4-Isopropylbenzoyl)benzoic acid

https://huagongshe.com/reaction/54865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantCumeneHCID 7406—
ReactantSodium CarbonateHCID 10340—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product2-(4-Isopropylbenzoyl)benzoic acidHCID 345798—

Reaction Steps

A mixture of 16 g (0.11 mol) phthalic anhydride, 30 g (0.22 mol) aluminum chloride and 12 g (0.10 mol) isopropylbenzene in 120 mL carbon disulfide was refluxed for 7 h in a water bath. The carbon sulfide was then removed by distillation. A dilute HCl solution (100 mL, 1.2N) was then added slowly to the remaining residue. The aqueous phase was decanted to yield a sticky solid. Na2CO3 aqueous solution (500 mL, 15%) was added slowly to the residue which resulted in considerable foaming. The solution was heated and the resultant solution was filtered to remove the undissolved material. The filtrate was acidified with conc. HCl to give an oily layer which was extracted with diethylether. The diethylether layer was dried with MgSO4, filtered and then the diethylether was removed by rotary evaporation to yield a cream-colored solid. The product was recrystallized from a 33/66 (v/v) mixture of toluene and pentane (17 g, 64%) mp 126°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624543
Source datasetuspto-grants-1997_04
ORD IDord-9a2b4ad822004b2db735e8a8cd072b2a
Source noteuspto-grants-1997_04