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A Manual of the Chemistry of the Carbon Compounds

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198 TEE GKEMISTRY OJf<br />

CHg.OCjjHgO<br />

Mthyl Acetylglycollate | .—Tliis e<strong>the</strong>r is obtained by<br />

CO.OCjjH,;<br />

heating ethyl monochloracetate with potassium acetate. It is a<br />

colourless liquid, having a pleasant fruity smell, and boiling at 179°.<br />

On distilling it with caustic potash it is resolved into potassium<br />

glycollate and acetic e<strong>the</strong>r. "When its aqueous solution is evaporated<br />

with slacked lime in vaeuo, calcium acetate, calcium glycollate, and<br />

calcium acetylglycolhte are produced: <strong>the</strong> latter salt crystallizes in<br />

small prisms.<br />

CO<br />

QlycoUUe or QlycoUic Anhydride | >O.—When glycollic acid is<br />

CHj<br />

heated above 150°, it is partially resolved into water and glycolHde.<br />

The latter compound is formed in larger quantity when potassium<br />

monochloracetate is heated to 120°. It is a white amorphous<br />

powder. When heated with water ifc is slowly reconverted into<br />

glycollic acid; this change takes place more quickly in <strong>the</strong> presence<br />

<strong>of</strong> an alkali.<br />

Diglycollu Add or Faramalic Acid.—O j GHTCO OH'" 11 " 3 bi "<br />

basic i acid id is i formed fod by b <strong>the</strong> th oxidation idti <strong>of</strong> f die<strong>the</strong>ne dih glycol l l as well ll as by b<br />

<strong>the</strong> dehydration <strong>of</strong> glycollic acid. It is also produced toge<strong>the</strong>r with<br />

glycollic acid when monochloracetic acid is boiled with milk <strong>of</strong> lime<br />

and calcium chloride. It forms large monoolinic crystals, and is very<br />

soluble in water. When it is heated -with fuming hydriodic acid it<br />

splits up into acetic acid and glycollic acid, and if <strong>the</strong> hydriodic<br />

acid be in excess <strong>the</strong> glycollio acid is also reduced to acetic acid:—-<br />

(1) O| CH*COOH + 2HI * HO.CHj.CQ.OH + 0HyCO.OH + I2<br />

/9« CIL.OH 0H8<br />

(

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