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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54721Erstellt: 23. Oktober 2026

Acetic Acid → 3,4-Diacetoxy-1-butene

https://huagongshe.com/de/reaction/54721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcetic AnhydrideHCID 7918—
EduktVinyloxiraneHCID 13586—
LösungsmittelDiglymeHCID 8150—
Produkt3,4-Diacetoxy-1-buteneHCID 273500111%

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

A 300-mL autoclave was charged with 40 mL (0.50 mol) of 3,4-epoxy-1-butene, 67.3 g (0.66 mol) acetic anhydride, 5.82 g (0.097 mol) of 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 2.5 hrs, samples were taken every 15 min for analysis by GC. GC analysis of the crude mixture after 2.5 hrs revealed 11% yield of 3,4-diacetoxy-1-butene with a 13% selectivity, 21% 3,4-epoxy-1-butene and numerous high boiling components. The reaction was observed to be first order in 3,4-epoxy-1-butene with a first order rate constant (Kfirst) of 0.0025 min-1 (Table A). This example illustrates low yield and selectivity in the absence of a tertiary amine and the inefficient catalysis of the reaction in the presence of the carboxylic acid alone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05623086
Quelldatensatzuspto-grants-1997_04
ORD IDord-7ecb83942ea440319dc3cf3eb9a62ee8
Quellennotizuspto-grants-1997_04