4-(Methylsulfonyl)phenylhydrazine hydrochloride
4-(Methylsulfonyl)phenylhydrazine hydrochloride Basic information
- Product Name:
- 4-(Methylsulfonyl)phenylhydrazine hydrochloride
- Synonyms:
-
- 4-METHYLSULPHONYLPHENYLHYDRAZINE HYDROCHLORIDE
- TIMTEC-BB SBB003335
- 4-(Methylsulfonyl)phenylhydrazine hydrochloride,95%
- 4-(Methylsulfonyl)phenylhydrazine hydrochloride
- 4-Hydrazino-1-(methylsulphonyl)benzene
- 4-Hydrazino-1-(methylsulphonyl)benzene hydrochloride
- 4-(Methylsulfonyl)phenylhydrazine hydrochloride, 95% 2.5GR
- (4-Methanesulfonyl-phenyl)-hydrazine hydrochloride
- CAS:
- 17852-67-4
- MF:
- C7H11ClN2O2S
- MW:
- 222.69
- Mol File:
- 17852-67-4.mol
4-(Methylsulfonyl)phenylhydrazine hydrochloride Chemical Properties
- Melting point:
- 202 °C
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- Crystalline Powder
- color
- Off-white to light yellow
- Water Solubility
- SOLUBLE
Safety Information
- Safety Statements
- 22-24/25
- HS Code
- 29280000
MSDS
- Language:English Provider:ACROS
4-(Methylsulfonyl)phenylhydrazine hydrochloride Usage And Synthesis
Chemical Properties
off-white to light yellow crystalline powder
Synthesis
5470-49-5
17852-67-4
General procedure for the synthesis of 4-(methylsulfonyl)phenylhydrazine hydrochloride from 4-methylsulfonylaniline: 100 mL of hydrochloric acid was added to a 500 mL four-necked flask, and the temperature inside the flask was cooled to -10 °C or lower by passing the flask through an ice-water bath and ensuring that the temperature did not exceed -10 °C. Subsequently, 10.27 g (0.06 mol) of 4-(methylsulfonyl)aniline was added and dissolved. After the exothermic reaction ceased, 4.47 g (0.065 mol) of sodium nitrite was slowly added and 30 g of distilled water was added dropwise over a period of 1 hour while keeping the temperature of the flask below -10°C. After completion of the addition, the addition of 67.7 g (0.30 mol) of tin chloride dihydrate dissolved in 60 mL of hydrochloric acid was continued dropwise over 1 h while the reaction temperature was strictly controlled at -10 °C or lower. Upon completion of the reaction, the solid product was collected by filtration and dried at 60 °C for 12 h using a vacuum drier to afford 4-(methylsulfonyl)phenylhydrazine hydrochloride (Intermediate G1). This step was based on a 67.9 mol% yield of 4-(methylsulfonyl)phenylhydrazine.
References
[1] Patent: JP2018/95798, 2018, A. Location in patent: Paragraph 0081; 0084
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