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HRID 256763Erstellt: 24. Oktober 2026

2-Chloro-1,1,1-trifluoroethane → Benzyl 2,2,2-trifluoroethyl sulfide

https://huagongshe.com/de/reaction/256763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-1,1,1-trifluoroethaneHCID 6408—
EduktBenzyl mercaptanHCID 7509—
EduktSodium HydroxideHCID 14798—
KatalysatorHexadecyltributylphosphonium bromideHCID 84716—
ProduktBenzyl 2,2,2-trifluoroethyl sulfideHCID 273779084%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A mixture of 1-chloro-2,2,2-trifluoroethane (20 g), benzyl mercaptan (12.4 g, 99% strength), sodium hydroxide (22.0 g of a 22% aqueous solution) and hexadecyl tributyl phosphonium bromide (0.51 g) was charged to a resealable Carius tube under a nitrogen atmosphere and heated at 70° C. for 10 hours. The tube was then cooled to 0° C., unsealed and the contents separated into two layers. The lower organic layer was collected, washed with water and purified by short path distillation to give 2,2,2-trifluoroethylthiomethylbenzene, b.p. 60°-70° C./ 10 mmHg, 17.4 g (yield 84%, strength 99%). The identity of the product was confirmed by gc-mass spectroscopy and nuclear magnetic reconance, and by comparison with data provided in C. Bunyagidj et al, J Org. Chem., 1981, 46 3335.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05258547
Quelldatensatzuspto-grants-1993_11
ORD IDord-3a7efd3878424318b295329d78bcf8e4
Quellennotizuspto-grants-1993_11