Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diglyme | HCID 8150 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Vinyloxirane | HCID 13586 | — |
| Edukt | Propionic anhydride | HCID 31263 | — |
| Produkt | 3,4-Dipropionyloxy-1-butene | HCID 21225102 | 84% |
Reaktionsschritte
A 100-mL autoclave was charged with 57.2 g (0.44 mol) propionic anhydride, 1.62 g (0.016 mol) of triethylamine and 3.44 g of diglyme. The autoclave was purged with helium twice, then the vessel was pressurized to 6.2 bars (75 psig) with helium followed by agitation. The reaction mixture was heated to 125° C., then 31.35 mL (0.40 mol) of 3,4-epoxy-1-butene was introduced to the reactor via syringe pump over 10 seconds. A first sample was taken at 1 min, then sequential samples were obtained every 15 min during the course of 2 hrs for analysis by GC. GC analysis of the crude mixture after 2 hrs revealed an 84% yield of 3,4-dipropionyloxy-1-butene with a 94% selectivity and 11.2% 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 use of another carboxylic anhydride with triethylamine and no carboxylic acid 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-8c0406fc12254a49995314db749bae9a |
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| Quellennotiz | uspto-grants-1997_04 |
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