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Difluoromethyl phenyl sulfone

Difluoromethyl phenyl sulfone structure

Difluoromethyl phenyl sulfone 

structure
  • CAS No:

    1535-65-5

  • Formula:

    C7H6F2O2S

  • Chemical Name:

    Difluoromethyl phenyl sulfone

  • Synonyms:

    [(Difluoromethyl)sulfonyl]benzene;Difluoromethyl phenyl sulfone;1-(difluoroMethylsulfonyl)benzene;Benzene, [(difluoroMethyl)sulfonyl]-;PhSO2CF2H;Phenyl difluoromethyl sulfone;Difluoromethyl phenyl sulfone >=97%;Difluoromethyl Phenyl Sulfone >

  • Categories:

    Organic Chemistry  >  Organic Fluorine Compound

Description

Difluoromethyl phenyl sulfone is a powerful nucleophilic difluoromethylation reagent due to the high reactivity of the sulfonyl-stabilized difluoromethyl anion towards many electrophiles including carbonyls, imines, alkyl halides, and cyclic sulfates and sulfamidates. In the nucleophilic reaction step, depending on the substrate structure, strong bases are used to generate the nucleophilic (phenylsulfonyl)difluoromethyl anion in situ. In the desulfonylation step, sodium/mercury amalgam and magnesium are the commonly used reductive reagents. Besides, the (phenylsulfonyl)difluoromethylated compounds can undergo β-elimination to afford gem-difluoroalkenes.


light yellow liquid

Difluoromethyl phenyl sulfone Basic Attributes

192.18

192.00565693

2259218

No

DTXSID60473498

colorless

29309090

Characteristics

1.348

24-25℃

115-120 °C(Press: 7 Torr)

1.5000

Soluble in chloroform and water.

under inert gas (nitrogen or Argon) at 2–8 °C

Safety Information

3

Xi

26-24/25

36/38

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

difluoromethyl phenyl sulfone

Difluoromethyl phenyl sulfone Use and Manufacturing

Efficient reagent for difluoromethylation of carbonyls and aldehydes.


Difluoromethyl Phenyl Sulfone has been used as a reagent for the nucleophilic difluoro(phenylsulfonyl)methylation of carbonyls

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