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・ N-sphere
・ N-Step-SCAN
・ N-Sub
・ N-substituted formamide deformylase
・ N-Succinimidyl 4-fluorobenzoate
・ N-succinylarginine dihydrolase
・ N-succinylornithine carbamoyltransferase
・ N-Sulfinyl imine
・ N-Sulfinylaniline
・ N-sulfoglucosamine sulfohydrolase
・ N-sulfoglucosamine-3-sulfatase
・ N-Terminal peptide of proopiomelanocortin
・ N-terminal prohormone of brain natriuretic peptide
・ N-terminal telopeptide
・ N-terminus
N-tert-Butylbenzenesulfinimidoyl chloride
・ N-Toon
・ N-topological space
・ N-Town Plays
・ N-Track Studio
・ N-Train
・ N-Trance
・ N-Trance discography
・ N-transform
・ N-Triples
・ N-tv
・ N-Tyce
・ N-type calcium channel
・ N-universes
・ N-up


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N-tert-Butylbenzenesulfinimidoyl chloride : ウィキペディア英語版
N-tert-Butylbenzenesulfinimidoyl chloride

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''N''-''tert''-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions. The nitrogen atom in the resulting intermediate is basic, and can abstract an α-hydrogen to create a new double bond.
== Preparation ==
''N''-''tert''-Butylbenzenesulfinimidoyl chloride can be synthesized quickly and in near-quantitative yield by reacting phenyl thioacetate with ''N''-''tert''-butyl-''N'',''N''-dichloroamine in benzene. After the reaction is complete, the product can be isolated as a yellow, moisture-sensitive solid by vacuum distillation.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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