ChemicalBook CAS DataBase List Cadmium stearate

Cadmium stearate synthesis

6synthesis methods

Product Name:Cadmium stearate
CAS Number:2223-93-0
Molecular formula:C18H36CdO2
Molecular Weight:396.9

506-82-1 Synthesis

506-82-1
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57-11-4 Synthesis

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2223-93-0
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Yield: 96.3%

Reaction Conditions:

in benzene

Steps:

5
Example 5 Synthesis of Cd(Stearate)₂; Within the glove box, a 500 mL three-neck round bottom flask was loaded with a stir bar and approximately 29.6 mmoles of Stearic Acid (8.4150 g). A glass stopper was connected to one neck, a 45 degree medium grain scintered frit with a 300 mL one-neck round bottom flask was connected to another neck and finally a high-vacuum line adapter was connected to the third neck. The reaction vessel was removed from glove box and immediately connected to the high-vacuum line. After a vacuum was established, approximately 200-250 mL of dry benzene was distilled into the reaction flask. Then the flask was transferred to a Schlenk line and backfilled with Argon. The glass stopper was replaced with a reflux condenser and the high-vacuum line adapter was replaced with a pressure-equalizing addition funnel capped with a rubber septa. The entire time an argon rich atmosphere was maintained, the exclusion of water and oxygen was the main priority. Before starting the reaction, a mark was placed on the pressure-equalizing addition funnel measuring 28 ml. Then via cannula transfer, about 28 mL of CdMe₂(14.0 mmoles) was added to the addition funnel. Once completed, the CdMe₂solution was slowly added to the reaction mixture over a period of 30-45 minutes. Throughout the addition the evolution of a gas is evident (Methane). Upon complete addition of the CdMe₂solution, the reaction vessel was set-up back to the original condition with high-vacuum line adapter and glass stopper and continuously stirred under a mild argon bubble. After 2 hours of stirring, a slight vacuum was established on the Schlenk line. Then the entire apparatus was place on the high-vacuum line where approximately half of the solvent was removed via flask to flask distillation. Then the resulting reaction mixture was filtered through frit and the volatile components were distilled back onto the crude product. This was repeated for a total of three times. Once completed, the remaining volatile components were removed on the high-vacuum line via flask to flask distillation. The product was left under dynamic vacuum overnight at which point the fine white powder was taken into the glove box and used. Yield 96.3%, ¹H NMR (d₆-benzene) T 55° C.: δ 7.15 (benzene), δ 2.04 (br, 2H), δ 1.49 (br, 2H), δ 1.29 (br, 20H), δ 0.903 (br, 3H).

References:

Lucey, Derrick W.;MacRae, David J.;Prasad, Paras N.;Beachley, Orville T. US2007/49765, 2007, A1 Location in patent:Page/Page column 6

57-11-4 Synthesis

57-11-4
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$6.00/100g