Organic Syntheses by Unknown
page 45 of 106 (42%)
page 45 of 106 (42%)
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[3b] J. Chem. Soc. 95, 235 (1909); Chem. News 98, 166 (1908).
[4b] Ber. 23, 752 (1890). [5b] Chem. News 66, 223 (1892). [6b] Ber. 27, 3292 (1894); [7b] Ber. 21, 2637 (1888). XI MESITYLENE 3 CH3COCH3 + (H2SO4)--> C6H3(CH3)3 +3H2O Prepared by ROGER ADAMS and R. W. HUFFERD. Checked by H. T. CLARKE and W. W. HARTMAN. 1. Procedure IN a 12-l. round-bottom flask, arranged so that the contents can be mechanically stirred, are placed 4600 g. (5750 cc.) of technical acetone. The flask is then well cooled with an ice-and-salt mixture, until the temperature of the acetone is between 0'0 and 5'0. Stirring is started, and 4160 cc. of commercial concentrated sulfuric acid is run in at such a rate that the temperature of the mixture never rises above about 10'0. |
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