The synthesis technique of Tosyl chloride: add chlorsulfonic acid and mixing sulfonation auxiliary agent in the there-necked flask that agitator, thermometer, gas distributor and condenser are housed; Be warming up to 50 ± 2 DEG C, keep this temperature, under the condition stirred, add ammonium chloride, be warming up …

How do you make tosyl chloride?

The synthesis technique of Tosyl chloride: add chlorsulfonic acid and mixing sulfonation auxiliary agent in the there-necked flask that agitator, thermometer, gas distributor and condenser are housed; Be warming up to 50 ± 2 DEG C, keep this temperature, under the condition stirred, add ammonium chloride, be warming up …

Is tosyl chloride toxic?

Inhalation May be harmful if inhaled. Causes respiratory tract irritation. Ingestion May be harmful if swallowed.

How do you remove tosyl chloride?

Tosyl chloride is soluble in hexanes; thus, it can be extracted by washing with hexanes, but this method is limited to products that are immiscible with hexanes. Chromatography is widely used, but it is slow and costly in terms of materials and time.

Is tosyl chloride an acid?

Reactions. Thus, tosylation followed by reduction allows for removal of a hydroxyl group. The resulting sulfonamides are non-basic and, when derived from primary amines, are even acidic. The preparation of tosyl esters and amides are conducted in the presence of a base, which absorbs hydrogen chloride.

Is TsCl an acid or base?

The resulting sulfonamides are non-basic and, when derived from primary amines, are even acidic. TsCl reacts with hydrazine to give p-toluenesulfonyl hydrazide. The preparation of tosyl esters and amides are conducted in the presence of a base, which absorbs hydrogen chloride.

Does tosyl chloride react with water?

Chemical dangers Decomposes on heating. This produces toxic and corrosive fumes including sulfur oxides and hydrogen chloride. Reacts with water and moist air. This produces hydrogen chloride (see ICSC 0163).

How is tosyl chloride removed from the reaction mixture?

Tosyl chloride can also be removed by its reaction with primary or secondary amines. 2 In this case the tosyl amides must be removed from solution. Finally tosyl chloride can be removed from solution by its reaction with a second excess hydroxyl source in the presence of a base.

How do you remove tosyl acid?

Tosyl acid itself water soluble.So we can give water wash to remove tosyl acid. if your product disolves in hexanes I would add hexanes and wash two times with saturated NaHCO3 as suggested above.

What is the purpose of pyridine?

Pyridines are important in medicinal chemistry because of their properties, which include weak basicity, water solubility, in vivo /chemical stability, hydrogen bond-forming ability, and small molecular size. Pyridine moieties are incorporated in many drugs and pesticides. Water solubility is one role of pyridines.