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HRID 1702504Erstellt: 24. Oktober 2026
Phthalic Acid → Diprop-2-en-1-yl 3,4,5,6-tetrachlorobenzene-1,2-dicarboxylate
https://huagongshe.com/de/reaction/1702504
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phthalic Acid | HCID 1017 | — |
| Edukt | Allyl chloride | HCID 7850 | — |
| Edukt | Diallyl phthalate | HCID 8560 | — |
| Edukt | HCID 20504075 | HCID 20504075 | — |
| Produkt | Diprop-2-en-1-yl 3,4,5,6-tetrachlorobenzene-1,2-dicarboxylate | HCID 22450728 | — |
Reaktionsschritte
Using a method similar to the known preparation of diallyl phthalate by reacting allyl chloride with metal salts of phthalic acid, Matsumoto et al prepared DATCP by reacting disodium tetrachlorophthalate with 2 moles of allyl chloride in an aqueous solution containing cuprous ions. Diallyl tetrachlorophthalate was also produced by Guseinov et al who reacted the anhydride with 3 moles of allyl alcohol plus 1 mole of hydrochloric acid in a benzene solution (Azerbaizhan Chemical Journal, No. 6, (1964), 21-23). Nordlander et al also produced DATCP by reacting the tetrachlorophthalic anhydride with 2 moles of allyl alcohol using sulfuric acid as a catalyst and driving off the water of reaction by distillation as an azeotrope with benzene (Journal of the American Chemical Society, 69, Nov., (1947), 2679-2682). However, only a 10% to 15% yield of the DATCP was obtained because of dehydration and polymerization reactions of the allyl alcohol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04381406 |
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| Quelldatensatz | uspto-grants-1983_04 |
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| ORD ID | ord-9e0fc8d2fa924861befa2fd30dd70fbd |
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| Quellennotiz | uspto-grants-1983_04 |
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