HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Terephthaloyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Chlorophenol | HCID 7245 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 87129072 | HCID 87129072 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Terephthaloyl chloride | HCID 7488 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436310 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-b259cb12f44e477aa89bd9ebfd72540d |
| Source note | uspto-grants-1995_07 |