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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27011Generated: October 25, 2026

Phthalic Anhydride → Dihydrochloride trihydrate

https://huagongshe.com/reaction/27011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantChlorobenzeneHCID 7964—
Reactant1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl-HCID 89715—
CatalystZincchlorideHCID 3007855—
ProductDihydrochloride trihydrateHCID 18760762—
Product2-(2,4-Bis(dimethylamino)benzoyl)benzoic acidHCID 20287212—

Reaction Steps

A mixture of phthalic anhydride (5.92 g.), N,N,N',N'-tetramethyl-m-phenylenediamine (6.56 g.), zinc chloride (5.40 g.) and chlorobenzene (70 ml.) was heated under reflux for three hours. The chlorobenzene was decanted and the residue was air-dried. A solution of the residue in dilute hydrochloric acid (10%, 20 ml. plus 20 ml. of water) was diluted with more water (20 ml.), affording 2-(2,4-bis-(dimethylamino)benzoyl)benzoic acid (II: Y'2 =Y'4 =(CH3)2N, Z4 =Z'5 =Z'6 =Z7 =H) dihydrochloride trihydrate (4 g., m.p. 136°-141° C.; after recrystallization from ethanol, m.p. 140°-141° C.). In another preparation the free base (m.p. 165°-168° C.) was obtained under less acidic conditions (pH 4-6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220357
Source datasetuspto-grants-1980_09
ORD IDord-d1c2a84a75f940b4858cb02ecc076c17
Source noteuspto-grants-1980_09