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 Synthesis of Pinacol hydrate
  • Synthesis of Pinacol hydrate
  • hydrate (CAS NO.: ) could be produced through many synthetic methods.

    Synthesis of Pinacol hydrate

    In a 5-l. round-bottomed flask, fitted with a stopper holding a separatory funnel and an efficient reflux condenser closed at the top with a calcium chloride tube, are placed 80 g. (3.29 atoms) of magnesium turnings and 800 cc. of dry benzene. Through the dropping funnel is added gradually a solution of 90 g. of mercuric chloride in 400 g. (505 cc., 6.9 moles) of acetone, carefully at first and then more rapidly after the reaction starts. The time of addition is about five to ten minutes. Sometimes the reaction does not commence until a considerable proportion of the acetone solution of mercuric chloride has been added. In this case the reaction proceeds very vigorously when it does start, and the flask must be cooled in running water to avoid loss through the condenser. As soon as the first vigorous reaction is over, a mixture of 200 g. (258 cc., 3.45 moles) of acetone and 200 cc. of benzene is added. When the reaction slows down, the flask is heated on a water bath until no further reaction is evident (about two hours). During this time the magnesium pinacolate swells until it fills the flask about three-fourths full. The flask is removed from the condenser and shaken until the reaction mass is well broken up. The condenser is again attached and the heating continued for another hour.

    Through the separatory funnel is then added 200 cc. of water, and the reaction mixture is heated for another hour. The flask should be shaken occasionally during this time. The reaction mixture is cooled to about 50° and filtered. The solid is returned to the flask and heated for ten minutes with a fresh 500-cc. portion of benzene to dissolve any remaining pinacol. The original filtrate and the second portion of benzene, after it is filtered from the magnesium hydroxide, are mixed and distilled to one-half the original volume in order to remove the acetone; the remaining benzene solution is treated with 300 cc. of water and cooled to 10–15°. The pinacol hydrate separates, and after about thirty minutes it is collected on a suction filter and washed with benzene, or better, the mixture is centrifuged in a basket centrifuge. The pinacol hydrate, air-dried at room temperature, weighs 325–375 g. (43–50 per cent of the theoretical amount based on the magnesium used). The product melts at 46–47°. It is sufficiently pure for most purposes. Occasionally the product is slightly yellow. If such a product is dissolved in an equal weight of boiling water, treated with a little animal charcoal, filtered, and the filtrate cooled in ice, over 95 per cent of the material may be recovered in large white crystals.


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