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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059245Generated: November 1, 2026

Benzoic Acid → HCID 20268295, compound

https://huagongshe.com/reaction/2059245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantEthanolHCID 702—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl-HCID 89715—
ProductHCID 20268295HCID 20268295—

Reaction Steps

In a procedure similar to that described above in part B of this example, 12.28 g (0.04 mole) of 2-[1-ethyl-2-methyl-3-indoly)carbonyl]benzoic acid, prepared as described in part A above, 8.57 g (0.05 mole) of N,N,N', N'-tetramethyl-m-phenylenediamine and 6.0 ml of acetic anhydride were interacted with stirring at room temperature overnight. The reaction mixture was then diluted with 13.0 ml of ethanol and the precipitate which separated was filtered and washed with 6.0 ml of ethanol. The filter cake was then reslurried in 30 ml of methanol, filtered and washed successively with methanol and diethylether. The material was dried in vacuo to obtain 15.8 g of 3-[2,4-bis(dimethylamino)phenyl]-3-(1-ethyl-2-methyl-3-indolyl)phthalide (Formula III: R°=R1 =R2 =R3 =Y1 =H; R=R5 =CH3 ; R4 =N(CH3)2 ; R6 =CH2CH3), a white crystalline solid which melted at 218°-222° C. The infrared spectrum was consistent with the structure. A benzene solution of the above product developed an intense grape-red color when streaked on a phenolic resin coated paper.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322352
Source datasetuspto-grants-1982_03
ORD IDord-a4ee2a8a8b0c4781bc7ea32c25181844
Source noteuspto-grants-1982_03