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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2413327Erstellt: 26. Oktober 2026

Ethyl Bromide → (Ethylthio)benzene

https://huagongshe.com/reaction/2413327

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktEthyl AcetateHCID 8857—
EduktHexamethylphosphoramideHCID 12679—
EduktPhenylthiotrimethylsilaneHCID 78312—
LösungsmittelWaterHCID 962—
Produkt(Ethylthio)benzeneHCID 1214483,3%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture of 11.52 g (63 mmoles) of phenylthio(trimethyl)silane, 22 ml of hexamethylphosphoric triamide and 18.8 ml (250 mmoles) of ethyl bromide was heated in a bath at 40° C. for 2 hours after which the conversion was complete. A solid formed in the reaction mixture and heating was continued for 1 hour after which the mixture was poured into a mixture of 150 ml of ethyl acetate and 50 ml of water. The ethyl acetate layer was separated and washed sequentially twice with 50 ml of water, 50 ml of a saturated sodium bicarbonate solution and twice with 25 ml of water. The combined water layers were extracted three times with 25 ml of ethyl acetate and the combined organic phases were washed twice with 25 ml of water, dried and evaporated to dryness. The residue was vacuum distilled to obtain 7.25 g (83% yield) of ethyl phenyl sulfide with a boiling point of 81.5°-84° C./14 mm Hg and a refractive index of nD25 =1.5632.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04496720
Quelldatensatzuspto-grants-1985_01
ORD IDord-945c78cf8e4447758b028a65bedabe2d
Quellennotizuspto-grants-1985_01