Reaktion #1264562

Reaktionsgleichung

water

4-fluorobenzenethiol

cyclopropyl bromide

t-BuONa

→

cyclopropyl(4-fluorophenyl)sulfane

Ausbeute 73.1%

Lösungsmittel

—

petroleum ether

DMSO

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturAfter cooled to room temperature
2. 2
   Extraktionextracted with diethyl ether (1.5 L×3)
3. 3
   WaschenThe combined organic phases were washed with water (1 L)
4. 4
   Trocknenbrine (1 L), dried over Na2SO4
5. 5
   Einengenconcentrated in vacuum

Vorschrift

To a stirred solution of 4-fluorobenzenethiol (134 g, 1.05 mol) in DMSO (3 L) under nitrogen atmosphere were added cyclopropyl bromide (140 g, 1.15 mol) and t-BuONa (138.7 g, 1.44 mol). Then the reaction mixture was heated to 80° C. and stirred for 2 days. TLC (petroleum ether) indicated the reaction was complete. After cooled to room temperature, the mixture was poured into water (2 L), extracted with diethyl ether (1.5 L×3). The combined organic phases were washed with water (1 L), then brine (1 L), dried over Na2SO4 and concentrated in vacuum to give cyclopropyl(4-fluorophenyl)sulfane (129 g, 73.1%) as a colorless oil. To a mixture of cyclopropyl(4-fluorophenyl)sulfane (129 g, 0.77 mol) and acetic acid (1.9 L) was added 30% H2O2 (1.2 L), and the mixture was heated to reflux and stirred overnight. TLC (petroleum ether:ethyl acetate=4:1) indicated the reaction was complete. After cooled to room temperature, the mixture was poured into water (1 L), then Na2S2O3 (200 g) was added to consume excess H2O2, then Na2CO3 was added to adjust pH=7. The mixture was extracted with ethyl acetate (1.5 L×2). The combined organic layers were washed with water (1 L), dried over Na2SO4 and concentrated in vacuum to give 69 g of crude product, which was purified by column chromatography (25% ethyl acetate in petroleum ether) to give the title compound (42 g, 27.3%) as a white solid.

Quelle