Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648666Generated: October 31, 2026

Dimethylformamide → Terephthaloyl chloride

https://huagongshe.com/reaction/1648666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-ChlorophenolHCID 7245—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 87129072HCID 87129072—
SolventDimethyl SulfoxideHCID 679—
SolventSulfuric AcidHCID 1118—
SolventChloroformHCID 6212—
ProductTerephthaloyl chlorideHCID 748898%

Reaction Steps

The bis-ester of Example 7 (3.9699 g, 0.079 mole) and terephthaloyl chloride (1.5836 g, 0.0078 mole) were polymerized by the procedure of Example 4. The amounts of aluminum chloride and DMF used were 9.19 g (0.0689 mole) and 2.40 mL (0.0312 mole), respectively. The polymer of the repeat unit ##STR24## was obtained as a pale cream powder in 98% yield. It was insoluble in a variety of solvents, including DMAc-lithium chloride (3%), o-chlorophenol, chloroform, and DMSO. It was soluble in concentrated sulfuric acid, but apparently with cleavage of the ester bonds, as the measured RV was only 0.07. DSC showed a possible Tg at 161° C. TGA in air showed a 1% weight loss at 380° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436310
Source datasetuspto-grants-1995_07
ORD IDord-b259cb12f44e477aa89bd9ebfd72540d
Source noteuspto-grants-1995_07