Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetyl chloride | HCID 6367 | — |
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Pivaloyl chloride | HCID 62493 | — |
| Edukt | Acrylic anhydride | HCID 74919 | — |
| Edukt | HCID 54295827 | HCID 54295827 | — |
| Produkt | Benzoic anhydride | HCID 7167 | — |
Reaktionsschritte
As seen below, benzoyl chloride, acetyl chloride and pivaloyl chloride were tested for use in the present invention. The best results were obtained with benzoyl chloride, which provided a yield of the acrylic anhydride of 77.2%. Acetyl chloride gave a less preferred product mixture that comprised 50% mixed anhydride, 25% acetic anhydride and 25% acrylic anhydride; the pivaloyl chloride reaction also gave a less preferred product mixture that comprised 50% mixed anhydride, 30% pivaloyl anhydride and 20% acrylic anhydride, based on gas chromatographic analysis. Benzoyl chloride is also more preferred than acetyl chloride and trimethyacetyl (pivaloyl) chloride, because the benzoyl chloride reaction yields benzoic anhydride which has a much greater boiling point than acrylic anhydride, facilitating the separation of the acrylic anhydride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05491244 |
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| Quelldatensatz | uspto-grants-1996_02 |
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| ORD ID | ord-cc463f6abaad48b9a0e88db179428b24 |
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| Quellennotiz | uspto-grants-1996_02 |
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