Identification | More | [Name]
CHLOROMETHYL PHENYL SULFONE | [CAS]
7205-98-3 | [Synonyms]
CHLOROMETHYL PHENYL SULFONE [(CHLOROMETHYL)SULFONYL]BENZENE PHENYL CHLOROMETHYL SULFONE [(chloromethyl)sulphonyl]benzene chloromethyl phenyl sulphone (Phenylsulfonyl)chloromethane Phenylsulfonylmethyl chloride | [EINECS(EC#)]
230-581-8 | [Molecular Formula]
C7H7ClO2S | [MDL Number]
MFCD00007551 | [Molecular Weight]
190.65 | [MOL File]
7205-98-3.mol |
Chemical Properties | Back Directory | [Melting point ]
51-53 °C (lit.) | [Boiling point ]
130 °C / 1mmHg | [density ]
1.336±0.06 g/cm3(Predicted) | [Fp ]
>230 °F
| [storage temp. ]
2-8°C
| [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) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
21 | [HS Code ]
29049095 |
Hazard Information | Back Directory | [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]
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 |
|
Company Name: |
Srisyn Labs
|
Tel: |
+91-9705168728 |
Website: |
www.srisyn.com |
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