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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398101Generated: October 31, 2026

Triethylamine → AcOH AcOAc

https://huagongshe.com/reaction/2398101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Chlorophthalic anhydrideHCID 67014—
SolventDimethylformamideHCID 6228—
ProductAcOH AcOAcHCID 21895370—

Reaction Conditions

Temperature50 °C

Reaction Steps

The procedure of Example 1 was repeated except that there was employed 3.0 parts of 4,4'-diphenyletherdithiol, 4.68 parts of 3-chlorophthalic anhydride, 2.85 parts of triethylamine and 38 parts of anhydrous DMF. The mixture was stirred at 50° C. for 3 hours to give a product which after acetic acid/acetic anhydride treatment consisted of a 93% yield of product. Recrystallization of this material from toluene/acetic anhydride gave a product in 87% yield, mp 224°-228° C. Based on the method of preparation the product was a thioetherdianhydride of the formula ##STR15##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024162
Source datasetuspto-grants-1977_05
ORD IDord-d2fab8b2c10447718b4311852a5f05d2
Source noteuspto-grants-1977_05