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CAFFEINE, or THEINE (1.3.7 trimethyl ...

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Originally appearing in Volume V04, Page 945 of the 1911 Encyclopedia Britannica.
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CAFFEINE, or THEINE (1.3.7 trimethyl 2 . 6 dioxypurin)  , C$ His N4 02 . H ? O, a substance found in the leaves and beans of the coffee tree, in tea, in
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Paraguay tea, and in small quantities in
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cocoa and in the
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kola nut . It may be extracted from tea or coffee by boiling with
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water, the dissolved tannin precipitated by basic lead acetate, the solution filtered, excess of lead precipitated by sulphuretted hydrogen and the filtered liquid then evaporated to crystallization; or, tea is boiled with water, and the whole then evaporated to a syrup, which is mixed with slaked lime, evaporated to dryness on the water-bath and extracted with chloroform (P . Cazeneuve, Bull. de la
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soc. chim. de Paris, 1876-1877, 27, p . 199) . Synthetically it may be prepared by the methylation of
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silver theobromine and silver theophyllin or by boiling heteroxanthine with methyl iodide and potash . E . Fischer and L . Ach (Berichte, 1895, 28, p . 3135) have synthesized it from dimethyl alloxan, whilst W . Traube (Berichte, 1900, 33, p .

3435) has obtained it from 1 . 3 diamethyl 4 . 5 diamino 2.6 dioxypyrimidine . On the constitution of

caffeine see BURIN and also E . Fischer (Annalen, 1882, 215, p . 253) . Caffeine crystallizes in long silky needles, which are slightly soluble in cold water . It becomes anhydrous at ro0° C. and melts at 234° to 23 5° C . It has a faint bitter taste and gives salts with
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mineral acids . On oxidation with nitric acid caffeine gives cholesterophane (dimethyl parabanic acid), but if chlorine water be used as the oxidant, then it yields monomethyl urea and dimethyl alloxan (E . Fischer) .

End of Article: CAFFEINE, or THEINE (1.3.7 trimethyl 2 . 6 dioxypurin)
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JACQUES CAFFIERI (1678-1755)

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