Identification | Back Directory | [Name]
4-(Methylsulfonyl)phenylhydrazine hydrochloride | [CAS]
17852-67-4 | [Synonyms]
TIMTEC-BB SBB003335 4-Hydrazino-1-(methylsulphonyl)benzene 4-METHYLSULPHONYLPHENYLHYDRAZINE HYDROCHLORIDE 4-(Methylsulfonyl)phenylhydrazine hydrochloride (4-Methanesulfonyl-phenyl)-hydrazine hydrochloride 4-(Methylsulfonyl)phenylhydrazine hydrochloride,95% 4-Hydrazino-1-(methylsulphonyl)benzene hydrochloride 4-(Methylsulfonyl)phenylhydrazine hydrochloride, 95% 2.5GR 1-Hydrazino-4-(methylsulphonyl)benzene hydrochloride, 4-Hydrazinophenyl methyl sulphone hydrochloride | [Molecular Formula]
C7H11ClN2O2S | [MDL Number]
MFCD00216494 | [MOL File]
17852-67-4.mol | [Molecular Weight]
222.69 |
Chemical Properties | Back Directory | [Appearance]
off-white to light yellow crystalline powder | [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 |
Hazard Information | Back Directory | [Chemical Properties]
off-white to light yellow crystalline powder | [Synthesis]
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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