![35951-28-1](/CAS/GIF/35951-28-1.gif)
2-CHLOROCYCLODODECANONE synthesis
- Product Name:2-CHLOROCYCLODODECANONE
- CAS Number:35951-28-1
- Molecular formula:C12H21ClO
- Molecular Weight:216.75
![CYCLODODECANONE](/CAS/GIF/830-13-7.gif)
830-13-7
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![2-CHLOROCYCLODODECANONE](/CAS/GIF/35951-28-1.gif)
35951-28-1
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Yield:35951-28-1 100%
Reaction Conditions:
Stage #1: cyclododecane-1-onewith n-butyllithium;N,N-diisopropylamine in tetrahydrofuran;hexane at -78; for 0.5 h;Inert atmosphere;
Stage #2: with Methyl chlorosulfonate in tetrahydrofuran;hexane at -78; for 0.5 h;Inert atmosphere;
Steps:
α-chlorination of ketones
General procedure: To a solution of diisopropylamine (170 μL, 1.2 eq.) in dry THF (2 mL) in a flame dried round bottom flask under argon at 0 °C was added n-butyllithium (690 μL, 1.6 M in hexanes, 1.1 eq.), and the reaction mixture was stirred at this temperature for 15 minutes. It was then cooled to -78 °C and a solution of ketone (1) (1 mmol) in THF (2 mL) slowly added. Stirring at -78 °C was continued for a further 30 minutes and methyl chlorosulfate (100 μL, 1.1 eq.) was then added. After stirring at -78 °C for 30 minutes, the reaction was quenched with an aqueous saturated ammonium chloride solution (5 mL). The mixture was then extracted with dichloromethane (3 x 5 mL), the combined organic phases were dried with anhydrous magnesium sulfate and the solvent evaporated under vacuum affording the desired α-chloroketone 2.
References:
Silva, Saúl;Maycock, Christopher D. [Tetrahedron Letters,2018,vol. 59,# 13,p. 1233 - 1238] Location in patent:supporting information
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35951-28-1
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![Cyclododecanone, 2-[(methylsulfonyl)oxy]-](/CAS/20210305/GIF/3667-85-4.gif)
3667-85-4
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35951-28-1
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121758-10-9
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![2-CHLOROCYCLODODECANONE](/CAS/GIF/35951-28-1.gif)
35951-28-1
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![CYCLODODECANONE](/CAS/GIF/830-13-7.gif)
830-13-7
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![cis-Cyclododecene.](/CAS/GIF/1129-89-1.gif)
1129-89-1
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![2-CHLOROCYCLODODECANONE](/CAS/GIF/35951-28-1.gif)
35951-28-1
41 suppliers
$45.00/50mg