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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Cumene | HCID 7406 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 2-(4-Isopropylbenzoyl)benzoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624543 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-9a2b4ad822004b2db735e8a8cd072b2a |
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| Source note | uspto-grants-1997_04 |
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