Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 2-(Phenylthio)aniline

2-(Phenylthio)aniline synthesis

12synthesis methods
-

Yield:1134-94-7 99%

Reaction Conditions:

with tetra(n-butyl)ammonium hydroxide;water;copper(l) chloride at 50; for 12 h;Inert atmosphere;

Steps:

General procedure for C-S coupling catalyzed by CuCl (procedure A):
General procedure: After standard cycles of evacuation and back-filling with dry and pure argon, an oven-dried Schlenk tube equipped with a magnetic stirring bar was charged with CuCl (5 mol%), the aryl iodides if a solid (1.2 equiv). The tube was evacuated and backfilled with argon (this procedure was repeated three times). Under a counter flow of argon, benzothiazole (0.5 mmol), aryl iodides if a liquid (1.2 equiv) and degassed 40% tetra-n-butylammonium hydroxides water solution (1.0 mL, 3.0 equiv) were added by syringe. The tube was sealed and the mixture was allowed to stir at 50 oC for 12 h. The reaction mixture was then allowed to cool to ambient temperature. Then, the mixture was quenched by the addition of a saturated NH4Cl solution (1.5 mL) and extracted with ethyl acetate (3×10 mL). Organic layers were gathered, dried over Na2SO4, filtered and concentrated in vacuum to yield the crude product. The obtained crude was purified by column chromatography on silica gel and the product was dried under vacuum for at least 0.5 h.

References:

Feng, Yi-Si;Qi, Hong-Xia;Wang, Wei-Cheng;Liang, Yu-Feng;Xu, Hua-Jian [Tetrahedron Letters,2012,vol. 53,# 23,p. 2914 - 2917] Location in patent:supporting information; experimental part

FullText

2-(Phenylthio)aniline Related Search: