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A Manual of the Chemistry of the Carbon Compounds

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38ff TBE CHEMISTRY OF<br />

base and an acid. By dry distillation, it yields phenol and o<strong>the</strong>r<br />

products; but, when heated very carefully, it is resolved into carbon<br />

dioxide and oxyphenyl-ethykmine C6H4(OH)C2H4.NH2> a white, crystalline<br />

sublimate, having an alkaline reaction, and forming crystellizable<br />

salts, Wheu tyxosine is fused with potash, it yields ammonia,<br />

acetic acid, and paraoxybenzoic acid; and when heated with hydriodic<br />

acid, it is resolved into ethyl-phenol (or an isomeride), carbon dioxide,<br />

and ammonia:—<br />

Tyrosins dissolves in hot sulphuric acid, yielding sulpho-acids,<br />

which are coloured violet by ferric chloride. On heating an aqueous<br />

solution <strong>of</strong> tyrosine with mercurious nitrate, it assumes a red colour,<br />

and <strong>the</strong>n a reddish-brown precipitate is formed.<br />

MelUotie Add, or Hydrocwmaric Acid C6H4 j n jx nn H' occur8<br />

in <strong>the</strong> yellow melilot {Mdilotws qfinnalis), and in <strong>the</strong> fragrant Fahatnleavea<br />

It crystallizes from water in large, pointed prisms, melting at<br />

82°, By distillation it is resolved into water and mclilotic anhydride<br />

C6H4 j Q TT >CO, a crystalline solid, melting at 25°, and boiling at<br />

272°. On fusing molilotic acid with potash, it yields acetic acid and<br />

salicylic acid.<br />

OXYPHENYL-ACRYLIC ACIDS.<br />

Paracttmaric Acid Q&JQH QQ H 5S P re P 8ted ^y exhausting<br />

aloes with dilute sulphuric acid, and treating <strong>the</strong> residue with e<strong>the</strong>r.<br />

It crystallizes from boiling water in brittle needles, melting at 180°.<br />

Nascent hydrogen converts it into hydroparaoumario acid.<br />

Cumaric Acid CJB.AQ n QQ H occurs t °g et l ier w Hli melildtic<br />

acid, and crystallizes from water in long needles, melting at 195°; by<br />

treating it with water aud sodinm.amalgam, it is converted into melilotic<br />

acid,<br />

Oumarin, or Cumaric Anhydride O6H4-j Q -U >CO, is found, com-<br />

bined with cumaric acid or melilotic acid, in <strong>the</strong> melilot and <strong>the</strong><br />

Faham-leaves, and exists in <strong>the</strong> free state in <strong>the</strong> Tonka-bean (Dipter&B<br />

odorata), in <strong>the</strong> sweet woodruff (Aspenda odwxtta), and in <strong>the</strong><br />

aweet-scented vernal grass {A-ntliomntkum, odoraLw).. It is readily<br />

obtained by exhausting tonka-beans with alcohol-, arid has been produced<br />

artificially by heating sodium-salicylaldehyde with acetic anhy-

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