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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8409Erstellt: 23. Oktober 2026

Benzyl Chloride → 1,4-Bis(benzyloxy)-2-butene

https://huagongshe.com/de/reaction/8409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl ChlorideHCID 7503—
Edukt2-Butene-1,4-diolHCID 8065—
EduktSodium HydroxideHCID 14798—
KatalysatorTetrabutylammonium BromideHCID 74236—
Produkt1,4-Bis(benzyloxy)-2-buteneHCID 4054109114,5%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To 48% aqueous sodium hydroxide (127.8 g) was added tetra-n-butylammonium bromide (3.3 g, 10 mmol). The mixture was heated to 60° C. To the mixture was added 2-butene-1,4-diol (17) (30.0 g, 340 mmol), to which was added dropwise benzyl chloride (94.8 g, 743 mmol) at 80±15° C. The mixture was stirred at the same temperature for 2 hours. The reaction mixture was cooled down, and separated after the addition of water (90 ml). To the organic layer was added sulfuric acidic brine. The solution was neutralized by aqueous sodium hydrogen carbonate, separated, mixed with ethyl acetate and concentrated under reduced pressure to yield the objective (18) (104.5 g, quantitative) as an oil residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087764B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-4caad36be5ac4269aa3917d91c05067e
Quellennotizuspto-grants-2006_08