Aniline → [(4-Aminophenyl)sulfanyl]formonitrile

To a -10° C., mechanically-stirred solution of aniline (21 g) and ammonium thiocyanate (52.1 g) in methanol (230 mL) was added a solution of bromine (38.7 g) in sodium bromide-saturated methanol. The rate of addition was adjusted such that the temperature of the reaction mixture did not rise above 0° C. After the addition was complete, the reaction mixture was stirred for one hour. The reaction mixture was then poured into a mixture of water (one liter), saturated aqueous sodium bicarbonate (500 mL) and ether (500 mL). The reaction mixture was then stirred for one hour and the phases separated. The organic phase was washed with brine, dried over magnesium sulfate and concentrated to yield an oil, which solidified upon trituration with hexane. The resulting solid was filtered and washed with hexane to afford 30.5 g of 4-thiocyanoaniline. Condensation of 4-thiocyanoaniline (5.7 g) with cyanoacetic acid, as described in Preparation 1, afforded 5.1 g of the title compound, α-cyano-4-thiocyanoacetanilide; m.p. 165°-166° C.

1. additionThe rate of addition
2. customdid not rise above 0° C
3. additionAfter the addition
4. stirringThe reaction mixture was then stirred for one hour
5. customthe phases separated
6. washThe organic phase was washed with brine
7. dry with materialdried over magnesium sulfate
8. concentrationconcentrated
9. customto yield an oil, which
10. filtrationThe resulting solid was filtered
11. washwashed with hexane

ORD 기록

ord-4d4a4348b065482e949d61c873861648

출처 데이터셋

uspto-grants-1991_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05034410