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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413882Generated: October 25, 2026

Phthalic Anhydride → 2-(2-Methyl-1-octyl-1H-indole-3-carbonyl)benzoic acid

https://huagongshe.com/reaction/1413882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
Reactant1H-Indole, 2-methyl-1-octyl-HCID 170708—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
Product2-(2-Methyl-1-octyl-1H-indole-3-carbonyl)benzoic acidHCID 1976380235.2%

Reaction Steps

In a manner similar to that described in part A of Example 1 hereinabove, 7.4 g (0.05 mole) of phthalic anhydride, 16.0 g (0.053 mole) of 76.5 percent active 1-n-octyl-2-methylindole, and 13.3 g (0.1 mole) of aluminum chloride were interacted in 50 ml of benzene to obtain 6.9 g of 2-[(1-n-octyl-2-methyl-3-indolyl)carbonyl]benzoic acid (Formula VIII: R0 =R1 =R2 =R3 =Y1 =H; R5 =CH3 ; R6 =(CH2)7CH3), as a pink-colored powder which melted at 121°-123° C. The nuclear magnetic spectrum was in agreement with the structure and a significant maxima occurred at 1717 cm-1 (C=O; s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251446
Source datasetuspto-grants-1981_02
ORD IDord-1c401d14a77c4c0e9af4cb625a3b3fcd
Source noteuspto-grants-1981_02