ChemicalBook--->CAS DataBase List--->42899-76-3

42899-76-3

42899-76-3 Structure

42899-76-3 Structure
IdentificationBack Directory
[Name]

PYRIDINE-3-SULFONYL CHLORIDE
[CAS]

42899-76-3
[Synonyms]

Pyridine-3-suL
TIMTEC-BB SBB010621
ASINEX-REAG BAS 13031029
PYRIDINE-3-SULFONYL CHLORIDE
Pyridine-3-sulfonyl chlor...
Pyridine-3-sulfonylchlorideHCl
Pyridine-3-Sulphonyl Chloride Hcl
3-(Chlorosulphonyl)pyridine hydrochloride
Pyridine-3-sulfonyl chloride hydrochloride ,95%
3-Pyridinesulfonylchloride, hydrochloride (1:1)
PYRIDINE-3-SULFONYL CHLORIDE ISO 9001:2015 REACH
Pyridine-3-sulfonyl chloride hydrochloride, tech
Pyridine-3-sulphonyl chloride hydrochloride, tech
[Molecular Formula]

C5H5Cl2NO2S
[MDL Number]

MFCD03452747
[MOL File]

42899-76-3.mol
[Molecular Weight]

214.07
Chemical PropertiesBack Directory
[Melting point ]

120-126
[Fp ]

>110℃
[storage temp. ]

Store below -20C
[Appearance]

white solid
[Water Solubility ]

Reacts with water.
[Sensitive ]

Moisture Sensitive
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

14-29-34
[Safety Statements ]

8-22-26-30-45-36/37/39
[RIDADR ]

UN 3265 8 / PGII
[Hazard Note ]

Corrosive/Keep Cold under -20C
[HazardClass ]

8
[HazardClass ]

IRRITANT
[HS Code ]

29333990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Phosphorus oxitrichloride-->Pyridine-->FUMING SULFURIC ACID-->MERCURY(II) SULFATE-->3-Pyridinesulfonic acid-->Chloroform-->Hydrochloric acid
[Preparation Products]

3-Pyridinesulfonamide-->5-phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Synthesis]

3-Pyridinesulfonic acid

636-73-7

Pyridine-3-sulfonyl chloride hydrochloride

42899-76-3

General procedure for the synthesis of pyridine-3-sulfonyl chloride hydrochloride from 3-pyridinesulfonic acid: 3-pyridinesulfonic acid (3.00 g, 18.8 mmol) was mixed with phosphorus pentachloride (PCl5, 4.79 g, 23.0 mmol) in phosphorus oxychloride (POCl3, 6 mL). The reaction mixture was stirred and reacted at 120°C overnight (15 h). After completion of the reaction, it was cooled to room temperature, diluted with chloroform (CHCl3, 20 mL) and saturated with hydrogen chloride gas (HCl(g)). The precipitated white precipitate was collected by filtration, washed with chloroform and dried under reduced pressure to give the title compound pyridine-3-sulfonyl chloride hydrochloride (3.36 g, 83% yield) as a white powder.

[References]

[1] Advanced Synthesis and Catalysis, 2004, vol. 346, # 8, p. 925 - 928
[2] Patent: WO2008/3703, 2008, A1. Location in patent: Page/Page column 82
[3] Patent: US2007/60623, 2007, A1. Location in patent: Page/Page column 24
[4] Patent: WO2006/36024, 2006, A1. Location in patent: Page/Page column 160
[5] Patent: EP2336107, 2015, B1. Location in patent: Paragraph 0306
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