Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Tributylamine | HCID 7622 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Vinyloxirane | HCID 13586 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | 3,4-Diacetoxy-1-butene | HCID 2735001 | 79% |
Reaktionsschritte
A 300-mL autoclave was charged with 40 mL (0.50 mol) of 3,4-epoxy-1-butene, 60.0 g (0.59 mol) acetic anhydride, 3.7 g (0.02 mol) of tributylamine, 0.72 g (0.012 mol) acetic acid and 4.2 mL of diglyme. The autoclave was purged with nitrogen twice, then the vessel was pressurized to 8 bars (100 psig) with nitrogen. The agitator was started and an initial sample was taken. The mixture was heated to 125° C. During the course of 2 hrs, samples were taken every 15 min for analysis by GC. GC analysis of the crude mixture after 2 hrs revealed a 79% yield of 3,4-diacetoxy-1-butene with a 90% selectivity and 12% 3,4-epoxy-1-butene. The reaction was observed to be first order in 3,4-epoxy-1-butene with a first order rate constant of 0.017 min-1 (Table A). This example shows the catalytic effect of another tertiary amine with acetic acid as the co-catalyst.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05623086 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-3aa2160cfd7d48bfb175aee0e666131a |
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| Quellennotiz | uspto-grants-1997_04 |
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