93366-52-0

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 120-78-5 di(benzothiazol-2-yl)disulfide 
• 1517-69-7 (R)-1-phenylethanol 
• 1445-91-6 (S)-1-phenylethanol 
• 149-30-4 2-Mercaptobenzothiazole 

Downstream Products

• 95091-04-6 Sodium; (R)-1-phenyl-ethanesulfinate 
• 2042-33-3 (R)-1-phenylethyl benzyl sulfone 
• 95-16-9 1,3-Benzothiazole 
• 95091-03-5 2-((R)-1-Phenyl-ethanesulfonyl)-benzothiazole 

Relevant academic research and scientific papers

A convenient method for the preparation of alkyl aryl sulfides from alcohols and (chloromethylene)dimethylammonium chloride

(Chloromethylene)dimethylammonium chloride (Vilsmeier reagent), prepared easily from DMF and oxalyl chloride, works as an efficient condensation reagent for the thioetherification of alcohols in one-pot under mild conditions. Various alcohols are successively converted into the corresponding sulfides with inversion of configurations in moderate to high yields. Copyright

ACTIVATION OF NITROSO GROUP WITH THIOLS. A NEW TRANSFORMATION OF PRIMARY AMINES TO ORGANIC SULFIDES OR THIOLS

Aliphatic primary amines reacted with 2-mercaptobenzothiazole in the presence of t-butylnitrite at room temperature to give condensation products, 2-(alkylthio)benzothiazole.

A CONVENIENT AND GENERAL SYNTHESIS OF ALKANE SULFINIC ACIDS

2-(Alkylsulfonyl)benzothiazoles are reduced with sodium tetrahydroborate to give alkane sulfinic acids in good yield.