戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 614563作成日:2026年10月26日

4-Amino-3-nitrophenyl thiocyanate → 4-(Benzylthio)-2-nitroaniline

https://huagongshe.com/reaction/614563

反応式

関与物質

役割名称HCID仕込み量
反応物4-Amino-3-nitrophenyl thiocyanateHCID 104677—
反応物Benzyl mesylateHCID 148757—
反応物Sodium borohydrideHCID 4311764—
溶媒DimethylformamideHCID 6228—
生成物4-(Benzylthio)-2-nitroanilineHCID 13550993—

反応手順

To a solution of 19.5 g (0.1 mol) 4-thiocyano-2-nitroaniline in 130 ml dimethylformamide is added 3.78 g (0.1 mol) sodium borohydride, all at once. The mixture is stirred for one-half hour, then 15.2 g (0.1 mol) benzyl methanesulfonate in 70 ml dimethylformamide is added. The solution is stirred at 30° for 3 hours, cooled and partitioned between water and dichloromethane. The layers are separated and the aqueous phase reextracted with dichloromethane. The organic phases are combined, washed with aqueous K2CO3, water and saturated NaCl, dried, filtered and stripped to yield 4-(benzyl)sulfenyl-2-nitroaniline.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04145433
出典データセットuspto-grants-1979_03
ORD IDord-9ca894cf666d453283d8aac483b14ef1
出典メモuspto-grants-1979_03