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N-tert-Butylbenzenesulfinimidoyl chloride : ウィキペディア英語版 | N-tert-Butylbenzenesulfinimidoyl chloride
}} ''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.
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