T=150°C; Yield given. Further byproducts given. Yields of byproduct given;
参考文献
Katritzky, Alan R.; Dega-Szafran, Zofia; Lopez-Rodriguez, Maria L.; King, Roy W.
Journal of the American Chemical Society, 1984 , vol. 106, # 19 p. 5577 - 5585
T=150°C; Yield given. Further byproducts given. Yields of byproduct given;
参考文献
Katritzky, Alan R.; Dega-Szafran, Zofia; Lopez-Rodriguez, Maria L.; King, Roy W.
Journal of the American Chemical Society, 1984 , vol. 106, # 19 p. 5577 - 5585
T=150°C; Yield given. Further byproducts given. Yields of byproduct given;
参考文献
Katritzky, Alan R.; Dega-Szafran, Zofia; Lopez-Rodriguez, Maria L.; King, Roy W.
Journal of the American Chemical Society, 1984 , vol. 106, # 19 p. 5577 - 5585
1: m-chloroperbenzoic acid / CH2Cl2 / 0.17 h / 20 °C 2: 30 percent / 70percent perchloric acid / 0.25 h / 20 °C View Scheme
参考文献
Cambie, Richard C.; Chambers, David; Lindsay, Barry G.; Rutledge, Peter S.; Woodgate, Paul D.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 822 - 827
3-chloro-benzenecarboperoxoic acid T=20°C; 1 h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
参考文献
Cambie, Richard C.; Chambers, David; Lindsay, Barry G.; Rutledge, Peter S.; Woodgate, Paul D.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 822 - 827
