CHLOROMETHYL PHENYL SULFONE
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
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)
MSDS
- Language:English Provider:SigmaAldrich
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
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CHLOROMETHYL PHENYL SULFONE(7205-98-3)Related Product Information
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