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CHLOROMETHYL PHENYL SULFONE

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CHLOROMETHYL PHENYL SULFONE Basic information

Product Name:
CHLOROMETHYL PHENYL SULFONE
Synonyms:
  • PHENYL CHLOROMETHYL SULFONE
  • CHLOROMETHYL PHENYL SULFONE
  • [(CHLOROMETHYL)SULFONYL]BENZENE
  • [(chloromethyl)sulphonyl]benzene
  • chloromethyl phenyl sulphone
  • Ai3-09778
  • Benzene, ((chloromethyl)sulfonyl)-
  • Einecs 230-581-8
CAS:
7205-98-3
MF:
C7H7ClO2S
MW:
190.65
EINECS:
230-581-8
Product Categories:
  • Organic Building Blocks
  • Sulfones
  • Sulfur Compounds
Mol File:
7205-98-3.mol
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CHLOROMETHYL PHENYL SULFONE Chemical Properties

Melting point:
51-53 °C (lit.)
Boiling point:
130 °C / 1mmHg
Density 
1.336±0.06 g/cm3(Predicted)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Almost white
BRN 
2046644
InChIKey
NXAIQSVCXQZNRY-UHFFFAOYSA-N
CAS DataBase Reference
7205-98-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
21
HS Code 
29049095

MSDS

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CHLOROMETHYL PHENYL SULFONE Usage And Synthesis

Uses

Chloromethyl Phenyl Sulfone is used to synthesis of α,β-epoxy sulfones and aziridines; reacts with electrophilic arenes, heterocyclic arenes, and alkenes; source of the α-phenylsulfonylmethyl radical.

Preparation

Preparative Methods of Chloromethyl Phenyl Sulfone: several methods are available. The most convenient is the reaction of Sodium Benzenesulfinate dihydrate with bromochloromethane in dimethyl sulfoxide.

Synthesis

100-68-5

3112-85-4

7205-98-3

The general procedure for the synthesis of phenylmethyl sulfone and chloromethyl phenyl sulfone from methyl phenyl sulfide was as follows: 0.25 g (2 mmol) of methyl phenyl sulfide was used as a substrate and added to a 50 mL three-necked flask along with 10 mL of acetonitrile and 2 mL of water. The internal temperature of the flask was maintained at 23 °C. Subsequently, 0.09 g (4.8 mmol) of sodium hypochlorite pentahydrate crystals were added in portions with continuous stirring. During the reaction, the internal temperature of the flask was increased to 28°C and then gradually decreased. GC analysis was performed 3 h after the start of the reaction and showed that 22% of the methyl phenyl sulfide was converted to methyl phenyl sulfoxide and 65% to methyl phenyl sulfone. By-products included 6% chloromethyl phenyl sulfoxide and 7% chloromethyl phenyl sulfone, and a total of 0.8% advanced chlorides. Addition of 0.79 g (4.8 mmol) of sodium hypochlorite pentahydrate crystals was continued and stirring was continued for 1 hour. At this point, the methyl phenyl sulfide and methyl phenyl sulfoxide completely disappeared and the yield of methyl phenyl sulfone increased to 87%. Impurities included 11% chloromethyl phenyl sulfone, 0.5% dichloromethyl phenyl sulfone and 1.3% trichloromethyl phenyl sulfone.

Solubility in organics

Chloromethyl Phenyl Sulfone is soluble in THF, CHCl3, CH2Cl2, and most organic solvents.

References

[1] Patent: JP2017/52730, 2017, A. Location in patent: Paragraph 0046

CHLOROMETHYL PHENYL SULFONESupplier

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