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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707147Generated: October 30, 2026

Acetic Anhydride → 3,3-Bis(2,4-bis(dimethylamino)phenyl)-5-(dimethylamino)phthalide

https://huagongshe.com/reaction/1707147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl-HCID 89715—
ReactantHCID 23343387HCID 23343387—
SolventHydrochloric AcidHCID 313—
Product3,3-Bis(2,4-bis(dimethylamino)phenyl)-5-(dimethylamino)phthalideHCID 54137693—

Reaction Steps

A mixture of 2-(2,4-bis(dimethylamino)benzoyl)-4-(dimethylamino)benzoic acid or the 5-(dimethylamino) isomer thereof (10 g.), N,N,N'-tetramethyl-m-phenylenediamine (2.30 g.) and acetic anhydride (50 ml.) was warmed (at 30°-35° C.) during one hour. More N,N,N',N'-tetramethyl-m-phenylenediamine (1.15 g.) was added and warming was continued. The mixture was diluted with dilute hydrochloric acid (10%) and ice and filtered. The filtrate was made alkaline. Crystallization of the product from toluene afforded 3,3-bis(2,4-bis(dimethylamino)phenyl)-5-(dimethylamino)phthalide (I: X=Y2 =Y4 =Z5 =(CH3)2N, Z4 =Z6 =Z7 =H) (m.p. 188°-192° C.) or the 6-(dimethylamino) isomer thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209618
Source datasetuspto-grants-1980_06
ORD IDord-807c1967fbf64e43aa0bef73564c1101
Source noteuspto-grants-1980_06