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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54723Erstellt: 23. Oktober 2026

Acetic Acid → 3,4-Diacetoxy-1-butene

https://huagongshe.com/de/reaction/54723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcetic AnhydrideHCID 7918—
EduktTriethylamineHCID 8471—
EduktVinyloxiraneHCID 13586—
LösungsmittelDiglymeHCID 8150—
Produkt3,4-Diacetoxy-1-buteneHCID 273500187%

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

A 300-mL autoclave was charged with 40 mL (0.50 mol) of 3,4-epoxy-1-butene, 62.2 g (0.61 mol) acetic anhydride, 1.8 g (0.018 mol) of triethylamine, 1.1 g (0.018 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 an 87% yield of 3,4-diacetoxy-1-butene with an 89% selectivity and 1.8% 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 0.024 min-1 (Table A). This example demonstrates the catalytic effect of the tertiary amine with acetic acid as the co-catalyst (Table B).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05623086
Quelldatensatzuspto-grants-1997_04
ORD IDord-d73b0011b14e4e15af10182136028344
Quellennotizuspto-grants-1997_04