Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Allyl chloride | HCID 7850 | — |
| Edukt | 4-Methoxyphenol | HCID 9015 | — |
| Edukt | Dimethyl Carbonate | HCID 12021 | — |
| Katalysator | Tetrabutylphosphonium bromide | HCID 76564 | — |
| Produkt | Carbonic acid, di-2-propen-1-yl ester | HCID 84764 | 3,4% |
| Produkt | Methyl 2-propen-1-yl carbonate | HCID 534788 | 25% |
Reaktionsschritte
The reaction conditions of Example 1 are substantially repeated employing allyl chloride (76.5 g, 1.0 mole), dimethyl carbonate (90.0 g, 1.0 mole), tetra-n--butylphosphonium bromide (6.78 g, 0.02 mole) and p-methoxyphenol (0.5 g, 0.004 mole) polymerization inhibitors. After heating for 7 hours at 150° C. and 600 psi carbon dioxide pressure, the reactor is cooled to room temperature and vented. Distillation gives 29.0 g (25 percent yield) of allyl methyl carbonate having b.p. of 79° C.-80° C. (150 torr) and 4.8 g (3.4 percent yield) of diallyl carbonate having b.p. of 107° C.-108° C. (150 torr).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04658041 |
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| Quelldatensatz | uspto-grants-1987_04 |
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| ORD ID | ord-fd00ddcaa05845dc807792b6bd347ae6 |
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| Quellennotiz | uspto-grants-1987_04 |
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