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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54725Erstellt: 24. Oktober 2026

Diglyme → 3,4-Dipropionyloxy-1-butene

https://huagongshe.com/de/reaction/54725

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiglymeHCID 8150—
EduktTriethylamineHCID 8471—
EduktVinyloxiraneHCID 13586—
EduktPropionic anhydrideHCID 31263—
Produkt3,4-Dipropionyloxy-1-buteneHCID 2122510284%

Reaktionsbedingungen

Temperatur125 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05623086
Quelldatensatzuspto-grants-1997_04
ORD IDord-8c0406fc12254a49995314db749bae9a
Quellennotizuspto-grants-1997_04