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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028352Generated: October 30, 2026

Phthalic Acid → Phthalic Anhydride

https://huagongshe.com/reaction/1028352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AcidHCID 1017—
ReactantSulfuric AcidHCID 1118—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTrifluoromethanesulfonic acidHCID 62406—
SolventTolueneHCID 1140—
ProductPhthalic AnhydrideHCID 681195%

Reaction Steps

As a method for producing a carboxylic anhydride, there have been known a reaction between a carboxylic acid and a carboxylic acid chloride and direct heating of a carboxylic acid. In the former case, since a large amount of hydrochloric acid is generated, a base in an amount in moles at least equivalent thereto must be used for neutralization, and hence the cost and time are increased. On the other hand, in the latter case, severe reaction conditions (300° C. or more) are required, and the yield is low. Besides those classical production methods, in Patent Document 1, a method for producing a phthalic anhydride derivative has been reported in which a dehydration reaction of a phthalic acid derivative is performed in an inert solvent in the presence of a catalytic amount of an acidic compound. As the acidic compound, for example, para-toluenesulfonic acid (p-TsOH), trifluoromethanesulfonic acid, polyphosphoric acid, and sulfuric acid are usable. For example, when phthalic acid was heated in toluene in the presence of a catalytic amount of p-TsOH under azeotropic reflux conditions with the removal of water, phthalic anhydride was obtained with a yield of 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735582B2
Source datasetuspto-grants-2014_05
ORD IDord-2d83d288377f4848880cfb878fff851e
Source noteuspto-grants-2014_05