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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449097Generated: November 1, 2026

Hydrochloric Acid → HCID 20098181, compound

https://huagongshe.com/reaction/1449097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl-HCID 89715—
ReactantHCID 12248790HCID 12248790—
ProductHCID 20098181HCID 20098181—

Reaction Steps

A mixture of 4.82 g (0.014 mole) of the 2-[(2-phenyl3-indolyl)carbonyl]benzoic acid from part A above, 3.60 g (0.02 mole) of N,N,N',N'-tetramethyl-m-phenylenediamine, and five ml of acetic anhydride was slowly heated until a purple color formed and maintained at this temperature for approximately two hours. After cooling to room temperature, sufficient 3N hydrochloric acid was added to the mixture to effect solution and stirring was continued for approximately 1.5 hours The resulting solution was filtered and the pH adjusted to five by the addition of sodium acetate. The precipitate which separated from the solution was collected by filtration and dried to obtain 3-[2,4-bis(dimethylamino)phenyl[-3-(2-phenyl-3-indolyl)phthalide (Formula III: R°=R1 =R2 =R3 =R6 =Y1 =H; R=CH3 ; R4 =N(CH3)2 ; R5 =C6H5 9. After recrystalization from toluene and hexane, the off white-colored solid melted at 153°-155° C. Significant infrared maxima were observed at 3380 cm-1 (NH; m) and 1750 cm-1 (C=O; s). The nuclear magnetic resonance spectrum was consistent with the structure. A toluene solution of this product spotted on silica gel developed an intense grape-red-colored image.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189171
Source datasetuspto-grants-1980_02
ORD IDord-e571c77141f344d3a1e7e8c4c2329257
Source noteuspto-grants-1980_02