Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381536Generated: November 2, 2026

Phthalic Anhydride → HCID 9913145, compound

https://huagongshe.com/reaction/1381536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantAcetic AnhydrideHCID 7918—
Reactant1H-Indole, 1-ethyl-2-methyl-HCID 170432—
ReactantBenzoic acid, 2-[(1-ethyl-2-methyl-1H-indol-3-yl)carbonyl]-HCID 3084978—
ReactantHCID 70399978HCID 70399978—
SolventWaterHCID 962—
ProductHCID 9913145HCID 9913145—

Reaction Steps

In a flask were charged 0.05 mol of m-diethyl-aminophenetidine and 0.05 mol of 3-(o-carboxybenzoyl)-1-ethyl-2-methylindole obtained by reacting 1-ethyl-2-methylindole and phthalic anhydride, and 0.3 mol of acetic anhydride was added thereto, followed by heating at 60° to 80° C. The reaction proceeded rapidly, and the reaction system assumed a bluish purple color. The reaction mixture was poured into water, and the precipitated crystals were collected by filtration and recrystallized from toluene to obtain the above-named compound having a melting point of 193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803192
Source datasetuspto-grants-1989_02
ORD IDord-0c901fef2f224c28af42f41cd2955d8f
Source noteuspto-grants-1989_02