Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chlorophthalic anhydride | HCID 67014 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | AcOH AcOAc | HCID 21895370 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04024162 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-d2fab8b2c10447718b4311852a5f05d2 |
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| Source note | uspto-grants-1977_05 |
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