Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7329Erstellt: 23. Oktober 2026

1,4-Dibromobutane → 3-[(4-Bromobutoxy)methyl]-3-ethyloxetane

https://huagongshe.com/de/reaction/7329

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DibromobutaneHCID 8056—
EduktHexaneHCID 8058—
EduktSodium HydroxideHCID 14798—
EduktOxt-101HCID 76444—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
Produkt3-[(4-Bromobutoxy)methyl]-3-ethyloxetaneHCID 2198931545%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Into a 2 L egg plant type flask were charged 46.3 g (0.40 mol) of 3-hydroxymethyl-3-ethyloxetane (product name: OXT-101 manufactured by Toagosei Co., Ltd.), 250.3 g (1.16 mol) of 1,4-dibromobutane (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.), and 275 ml of hexane. 500 ml of a 33% sodium hydroxide aqueous solution containing 2 g of tetra-n-butylammonium bromide (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added to the mixture and vigorously stirred for 5 hours. After the mixture was refluxed at a temperature of 80° C. for one hour, 500 ml of deionized water was added thereto so as to separate the mixture into an organic phase and an aqueous phase. The aqueous phase was extracted three times with 160 ml of hexane. After the organic phase and the extracted phase were dried over magnesium sulfate, the solvent was distilled out in a vacuum. The resulting transparent liquid was distilled in a vacuum thereby obtaining 44.5 g (0.18 mol) of 3-[(4-bromobutoxy)methyl]-3-ethyloxetane as a distillate at 109° C./532 Pa (yield: 44%, identified with 1H-NMR).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087273B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-9bdd41d1c9294f7b851c289c0070b4ce
Quellennotizuspto-grants-2006_08