HRID351888

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID70297

Benzenecarboperoxoic acid, 3-chloro-

C7H5ClO3

结构：CCSc1ccc(N2C[C@@H](CN=[N+]=[N-])OC2=O)cc1F

HCID22966212

未命名化合物

结构：CS(=O)c1ccc(N2C[C@@H](CN=[N+]=[N-])OC2=O)cc1F

HCID22966213

未命名化合物

PRODUCTS

生成物

结构：CCS(=O)c1ccc(N2C[C@@H](CN=[N+]=[N-])OC2=O)cc1F

HCID22966211

未命名化合物

PROCEDURE

实验过程

This compound was prepared analogously to the synthesis of 5-(S)-azidomethyl-3-[4′-methylsulfinyl-3′-fluorophenyl]oxazolidine-2-one from 5-(S)-azidomethyl-3-[4′-ethylthio-3′-fluorophenyl]oxazolidine-2-one (0.250 g, 0.844 mmol) and m-chloroperoxybenzoic acid (77%, 0.189 g, 0.844 mmol). Yield 0.235 g (89%). MS (m/z): [M+H]+=313.