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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1602683Erstellt: 26. Oktober 2026

Acetic Acid → Butane-2,3-diyl diacetate

https://huagongshe.com/reaction/1602683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktOxygenHCID 977—
Edukt1,3-ButadieneHCID 7845—
ProduktButane-2,3-diyl diacetateHCID 66193—

Reaktionsschritte

The conventional butadiene process starts with reaction of butadiene with acetic acid and oxygen-containing gas, followed by hydrogenation to obtain diacetoxybutane (see FIG. 1). As shown in FIG. 2, the resulting diacetoxybutane is hydrolyzed, and acetic acid and water are distilled off from the liquid reaction mixture containing crude 1,4-butanediol (hydrolyzate) in a first distillation tower. Diacetoxybutane and hydroxyacetoxybutane are separated from the hydrolyzate in a second distillation tower. The resulting crude 1,4-butanediol is hydrogenated with hydrogen gas in the presence of a catalyst for hydrogenation. After tetrahydrofuran (hereinafter abbreviated as THF) is concentrated in a third distillation tower, high purity 1,4-butanediol is recovered from a fourth distillation tower as a side stream or a bottom.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05981810
Quelldatensatzuspto-grants-1999_11
ORD IDord-8183195a9f684fb5a4c60f409efa4639
Quellennotizuspto-grants-1999_11