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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 889682Erstellt: 23. Oktober 2026

Tetrahydrothiophene → 2-Phenyl-1-oxaspiro[2.5]octane

https://huagongshe.com/de/reaction/889682

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrothiopheneHCID 1127—
EduktBenzyl ChlorideHCID 7503—
EduktCyclohexanoneHCID 7967—
EduktPotassium HydroxideHCID 14797—
EduktS-benzyltetrahydrothiophenium chlorideHCID 86626231—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt2-Phenyl-1-oxaspiro[2.5]octaneHCID 25481481,5%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A mixture of 152 g (1.18 mol) of benzyl chloride, 108 g (1.18 mol) of tetrahydrothiophene and 0.225 L of water is stirred well at 85° C. until a homogeneous clear or slightly turbid single-phase solution of S-benzyltetrahydrothiophenium chloride has been obtained. The solution is cooled to 20° C. and is slowly added dropwise to a reaction mixture consisting of potassium hydroxide solution (prepared from 267 g (4.75 mol) of potassium hydroxide in 0.53 L of ice-water) and 467 g of cyclohexanone (4.75 mol) in 225 g of methanol. After the addition is complete, the reaction mixture is allowed to stand for 10 minutes until the phases have separated; the organic phase is separated off and subjected to fractional distillation. 181 g (80%) of 2-phenyl-1-oxa-spiro[2.5]octane are obtained in the form of a clear colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08252959B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-a08d88969042452693127dbad0239381
Quellennotizuspto-grants-2012_08