反应详情

温度

50 °C

A mixture of 6.0 gm (0.0224 mol) of (E)-2-[(methylamino)phenylmethylene]-benzo[b]thiophen-3(2H)-one, 100 ml of glacial acetic acid and 3.5 ml (0.034 mol) of an aqueous 30% hydrogen peroxide solution was heated at 50° C. for four hours while stirring and then allowed to stand overnight at room temperature. After the addition of 40 ml of a 10% sodium sulfite solution, the mixture was concentrated by evaporation in vacuo, and the residue was suspended in 200 ml of water. The solid material precipitated thereby was suction-filtered off and then broken down into its constituents by column chromatography on 300 gm of silica gel, using 1,2-dichloroethane/ethyl acetate (97:3 v/v) as the eluant. By evaporating the appropriate fractions, 2.0 gm (33% of theory) of pale yellow (E)-2-[(methylamino)phenylmethylene]-benzo[b]thiophen-3(2H)-one-1-oxide, m.p. 205-206° C (decomposition) from ethanol), and 0.10 gm (1.5% of theory) of light yellow (E)- 2-[(methylamino)phenylmethylene]-benzo[b]-thiophen-3(2H)-one-1,1-dioxide, m.p. 302°-303° C., were obtained.

1. concentrationthe mixture was concentrated by evaporation in vacuo
2. customThe solid material precipitated
3. filtrationthereby was suction-filtered off
4. customBy evaporating the appropriate fractions, 2.0 gm (33% of theory) of pale yellow (E)-2-[(methylamino)phenylmethylene]-benzo[b]thiophen-3(2H)-one-1-oxide, m.p. 205-206° C (decomposition) from ethanol), and 0.10 gm (1.5% of theory) of light yellow (E)- 2-[(methylamino)phenylmethylene]-benzo[b]-thiophen-3(2H)-one-1,1-dioxide, m.p. 302°-303° C.
5. customwere obtained