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| | 4-Chloroformylphthalic anhydride Basic information |
| Product Name: | 4-Chloroformylphthalic anhydride | | Synonyms: | 1,3-Benzofurandione-5-carbonyl chloride;1,3-dihydro-1,3-dioxo-5-isobenzofurancarbonylchlorid;1,3-Dioxo-1,3-dihydro-2-benzofuran-5-carbonyl chloride;4-(Chlorocarbonyl)phthalic anhydride;4-(Chlorocarboxy)benzenedicarboxylic anhydride;5-Isobenzofurancarbonyl chloride, 1,3-dihydro-1,3-dioxo-;5-Isobenzofurancarbonylchloride,1,3-dihydro-1,3-dioxo-;Anhydrotrimellitic acid chloride | | CAS: | 1204-28-0 | | MF: | C9H3ClO4 | | MW: | 210.57 | | EINECS: | 214-874-8 | | Product Categories: | Fluorenes, etc. (reagent for high-performance polymer research);Functional Materials;Reagent for High-Performance Polymer Research | | Mol File: | 1204-28-0.mol |  |
| | 4-Chloroformylphthalic anhydride Chemical Properties |
| Hazard Codes | C | | Risk Statements | 34-29 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 3261 8/PG 2 | | WGK Germany | 3 | | F | 10-21 | | TSCA | TSCA listed | | HazardClass | 8 | | PackingGroup | II | | HS Code | 29173990 |
| | 4-Chloroformylphthalic anhydride Usage And Synthesis |
| Chemical Properties | white crystalline solid | | Uses | Trimellitic Anhydride Chloride can be used as a reagent to synthesize optical polyamideimides. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 38, p. 2557, 1973 DOI: 10.1021/jo00954a034 | | Flammability and Explosibility | Not classified | | Synthesis | The general procedure for the synthesis of 1,3-dioxo-1,3-dihydroisobenzofuran-5-carbonyl chloride from trimellitic anhydride was as follows: trimellitic anhydride (50 g) and cyclohexane (45 mL) were added to a reaction flask containing 4-dimethylaminopyridine (0.05 g), and heated to 90 °C. Subsequently, thionyl chloride (37.2 g, molar ratio of trimellitic anhydride to thionyl chloride 1:1.2) was added slowly and the reaction mixture was refluxed for 6 hours. Upon completion of the reaction, it was confirmed that no gas was produced. At the end of the reaction, the remaining cyclohexane and excess thionyl chloride were removed by distillation at 90 °C and the solution was recovered at -0.085 MPa. Next, the 180-190 °C fraction was collected by vacuum distillation (vacuum of 750 mmHg) to give trimellitic anhydride chloride (47.6 g). After cooling, the product was a white solid with a melting point of 67.5~68.8 °C, and the HPLC purity was 99.5% in 86.9% yield. | | References | [1] Patent: CN103626729, 2016, B. Location in patent: Paragraph 0026; 0027
[2] Patent: CN106748963, 2017, A. Location in patent: Paragraph 0048; 0049; 0050; 0051
[3] Patent: CN108341796, 2018, A. Location in patent: Paragraph 0016; 0017; 0018; 0019; 0020; 0021
[4] Patent: US10093929, 2018, B2. Location in patent: Page/Page column 2-3 |
| | 4-Chloroformylphthalic anhydride Preparation Products And Raw materials |
| Raw materials | Trimellitic Anhydride-->Thionyl chloride-->Cyclohexane-->4-Dimethylaminopyridine | | Preparation Products | 5-Isobenzofurancarboxylic acid, 1,3-dihydro-1,3-dioxo-, 5,5'-[(1-methylethylidene)di-4,1-phenylene] ester-->5-Iodoisobenzofuran-1,3-dione-->5-(3-phenylprop-2-ynoyl)-1,3-dihydro-2-benzofuran-1,3-dione-->1,4-dichlorophthalazine-6-carbonitrile-->4-Butyloxycarbonyl-1,2-benzenedicarboxylic anhydride-->p-phenylenebis(trimellitate anhydride)) |
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