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Flasks Grignard

Method 2. Equip a 1 htre thre necked flask with a double surface reflux condenser, a mechanical stirrer and a separatory funnel, and place 12 -2 g. of dry magnesium turnings, a crystal of iodine, 50 ml. of sodium-dried ether and 7-5 g. (5 ml.) of a-bromonaphthalene (Section IV,20) in the flask. If the reaction does not start immediately, reflux gently on a water bath until it does remove the water bath. Stir the mixture, and add a solution of 96 g. (65 ml.) of a-bromonaphthalene in 250 ml. of anhydrous ether from the separatory funnel at such a rate that the reaction is vmder control (1 -5-2 hours). Place a water bath under the flask and continue the stirring and refluxing for a further 30 minutes. The Grignard reagent collects as a heavy oil in the bottom of the flask ... [Pg.765]

The receiving flask contents should contain a very pure product. There is no need to clean up any further. For the next stage however they wilt need to be dried over sodium sulphate. This can either be done now or later. Now is better, dry your product before you weigh it and place it in a screw capped bottle ready for the Grignard reaction. [Pg.228]

After the air in the flask had been replaced completely with nitrogen, 100 ml of dry diethyl ether, 0.20 mol of the cumulenic ether (see Chapter V, Exps. 7, 8 and 11) and 1 g (note 1) of copper(l) bromide were placed in it. A solution of the Grignard-reagent, prepared from 0.50 mol of the chloride (see Chapter II,... [Pg.187]

D. a-Allyl- -bromoelhyl ethyl ether. The same apparatus is used as in the preparation of allylmagnesium bromide. The flask is charged with an amount of the Grignard solution (part C) equivalent to 2.78 moles of allylmagnesium bromide (or chloride) and cooled in an ice bath. A solution of 580 g. (2.5 moles) of o , 3-dibromoethyl ethyl ether (part B) in an equal volume of anhydrous ether is added slowly with stirring over a period of 3-4 hours. The mixture is allowed to stand overnight and is then hydrolyzed with 75 ml. of 20% acetic acid followed by 500 ml. of water. The ether layer is separated, washed with four 100-ml. portions of 10% aqueous sodium bicarbonate solution followed by four 100-ml. portions of saturated aqueous sodium chloride solution, dried over 100 g. of anhydrous calcimn sulfate, and distilled under reduced pressure. The yield of colorless a-allyl-/3-bromoethyl ethyl ether is 370-396 g. (77-82% based on the a, 3-dibromoethyl ethyl ether), b.p. 72-75°/21 mm., 1.4600-1.4606. [Pg.62]

The Grignard reaction starts within a few minutes and should not require the use of a catalyst If the reaction has not commenced within 5 minutes, the flask should be gently heated with a hot water bath until reaction starts... [Pg.50]


See other pages where Flasks Grignard is mentioned: [Pg.284]    [Pg.51]    [Pg.240]    [Pg.252]    [Pg.252]    [Pg.254]    [Pg.256]    [Pg.259]    [Pg.359]    [Pg.359]    [Pg.756]    [Pg.756]    [Pg.785]    [Pg.813]    [Pg.814]    [Pg.875]    [Pg.878]    [Pg.936]    [Pg.233]    [Pg.233]    [Pg.235]    [Pg.236]    [Pg.238]    [Pg.246]    [Pg.1]    [Pg.14]    [Pg.15]    [Pg.158]    [Pg.160]    [Pg.160]    [Pg.166]    [Pg.393]    [Pg.49]    [Pg.86]    [Pg.61]    [Pg.87]    [Pg.108]    [Pg.208]    [Pg.149]    [Pg.251]    [Pg.727]    [Pg.1020]    [Pg.55]    [Pg.49]    [Pg.128]    [Pg.72]   
See also in sourсe #XX -- [ Pg.51 ]

See also in sourсe #XX -- [ Pg.51 ]

See also in sourсe #XX -- [ Pg.51 ]




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