戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 864747作成日:2026年10月25日

Benzyl Bromide → 2-benzyl-4-isopropyl-6-(N,N-diethylthiocarbamyloxy)saccharin

https://huagongshe.com/reaction/864747

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Diethylthiocarbamoyl chlorideHCID 66607—
反応物CesiumHCID 5354618—
反応物4-Isopropyl-6-hydroxysaccharinHCID 10037346—
反応物2-Benzyl-4-isopropyl-6-hydroxysaccharinHCID 70044650—
溶媒DimethylformamideHCID 6228—
生成物2-benzyl-4-isopropyl-6-(N,N-diethylthiocarbamyloxy)saccharinHCID 86746562—

反応手順

Selective N-benzylation of the cesium salt of 4-isopropyl-6-hydroxysaccharin (Preparation 19) with benzyl bromide and reaction of the 2-benzyl-4-isopropyl-6-hydroxysaccharin with N,N-diethylthiocarbamyl chloride in DMF using the procedure described above in Preparation 12 affords 2-benzyl-4-isopropyl-6-(N,N-diethylthiocarbamyloxy)saccharin which, on heating, rearranges to 2-benzyl-4-isopropyl-6-(N,N-diethylcarbamyl-thio)saccharin. The latter, on hydrolysis with alkali, affords 2-benzyl-4-isopropyl-6-mercaptosaccharin which on reaction with methyl iodide, and transfer hydrogenolysis affords 4-isopropyl-6-methylthiosaccharin. Oxidation of the latter with one or two molar equivalents of 3-chloroperbenzoic acid affords 4-isopropyl-6-methyl-sulfinylsaccharin and 4-isopropyl-6-methulsulfonyl-saccharin.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05563163
出典データセットuspto-grants-1996_10
ORD IDord-0efe7b337a8d4b5586f61a2696e231d6
出典メモuspto-grants-1996_10