Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Chlorophthalic anhydride | HCID 67014 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | Phthalic Anhydride | HCID 6811 | — |
Reaction Steps
In the “In Situ ClPAMI” procedure, the five-necked flask setup described above was used. The ClPAMI was synthesized in the five-necked flask by reacting two moles of chlorophthalic anhydride with one mole of mPD using oDCB as solvent. The water formed was removed by distillation until a moisture content of less than 20 ppm in the distillate was obtained. Then, HEGCl, a phase transfer catalyst, was added in an amount of 0.6 weight %, based on the ClPAMI amount. More oDCB was distilled off to confirm that the moisture level was less than 20 ppm in the distillate. Then, a slurry of Na2BPA and NaPCP in oDCB in the second flask was transferred to the five-necked flask using the addition tube in communication with the second flask, and polymerization was conducted at 180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193829B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8d2255d7360c4be6a71cde849149c034 |
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| Source note | uspto-grants-2015_11 |
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