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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051733Generated: October 30, 2026

Phthalic Anhydride → Benzoic acid, 2-[(1-butyl-2-methyl-1H-indol-3-yl)carbonyl]-

https://huagongshe.com/reaction/2051733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
Reactant1H-Indole, 1-butyl-2-methyl-HCID 3084883—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
ProductBenzoic acid, 2-[(1-butyl-2-methyl-1H-indol-3-yl)carbonyl]-HCID 105559—

Reaction Steps

To a stirred mixture containing 7.4 g. of phthalic anhydride and 16.0 g. of 1-butyl-2-methylindole at 0°-5° C. was added portionwise 13.3 g. of aluminum chloride. The mixture was diluted with 50 ml. of benzene and stirred overnight at room temperature. The reaction mixture was poured into 200 ml. of 5% hydrochloric acid and the product extracted with benzene. The benzene extracts were shaken with dilute aqueous potassium hydroxide. The aqueous alkaline layer was separated, cooled with ice and brought to pH 4 with acetic acid. The precipitated product was collected and dried to give 2-(1-butyl-2-methyl-3-indolylcarbonyl)benzoic acid, m.p. 88°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182714
Source datasetuspto-grants-1980_01
ORD IDord-f2a9450cd3744c658ba102d80e665897
Source noteuspto-grants-1980_01