sodium sulfide; hydrogenchloride; zinc; n,n-dimethyl-formamide; water;
reactants are commercially availlable.
tetrahedron letters, vol. 53, 20, (2012), p. 2548 - 2551 general procedure: into an oven-dried flask equipped with a magnetic stir bar was added aryl fluoride (1.00 g, 1.0 eq.), na2s (1.1 eq.) and dmf (5 ml) under argon. the reaction mixture was stirred at room temperature for 1 h. then 1 m naoh (50 ml) was added and was washed with ch2cl2 (2 x 25 ml). the aqueous layer was acidified to ph ~ 1-2 with 6 n hcl and extracted with ch2cl2 (2 x 50 ml). the co mbined organic layer was washed with brine (50 ml), dried over mgso4, filtered and concentrated under reduced pressure to provide a crude residue. to the residue was added 10percent hcl (40 ml) and co oled with an ice-water bath. then zinc dust (4 g) was added and the mixture was stirred for 1 h. then etoac (100 ml) was added and the mixture was stirred for an additional 30 minutes. the organic lay er was separated and washed with water (40 ml) and brine (40 ml), dried over mgso4, filtered and concentrated to provide the desired product with satisfactory purity.
feel free to call us on
drop us a line anytime at
and we’ll get back soon.
come visit us at 南京市江宁区科学园乾德路5号