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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660274Generated: November 1, 2026

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

https://huagongshe.com/reaction/1660274

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

Following the procedure described in part A of Example 1, 7.4 g (0.05 mole) of phthalic anhydride, 16.0 g (0.07 mole) of 79 percent active 1-n-butyl-2-methylindole and 13.3 g (0.01 mole) of aluminum chloride were interacted in 50 ml of benzene to obtain 2[(1-n-butyl-2-methyl-3-indolyl)carbonyl]benzoic acid (Formula VIII: Ro =R1 =R2 =R3 =Y1 =H; R5 =CH3 ; R6 =(CH2)3CH3) a pale pink solid melting over the range 88°-92° C. The nuclear magnetic resonance spectrum was consistent with the structure. Infrared maxima were recorded at 1720 cm-1 (C=O; s) and 1700 cm31 1 (C=O; s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307018
Source datasetuspto-grants-1981_12
ORD IDord-40fc1b93fb2441af85e675f25477e449
Source noteuspto-grants-1981_12