HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Sulfur Dioxide → Sulfur Dioxide

HRID 534690
Notes
Print preview

Reaction equation

HRID 534690 reaction equation
[S:1](=[O:3])=[O:2].[C:4]1([S:10][C:11]([Si](C)(C)C)([F:13])[F:12])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[F-].[Cs+].[B-](F)(F)(F)[F:21].[B-](F)(F)(F)F.C1[N+]2(CCl)CC[N+](F)(CC2)C1>C(#N)C>[S:1](=[O:3])=[O:2].[F:12][C:11]([F:13])([S:10][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[S:1]([F:21])(=[O:3])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 1119Sulfur DioxideHCID 25953Cesium fluorideHCID 2724933SelectfluorHCID 11075297HCID 11075297, compound2×

Product 2

HCID 1119Sulfur DioxideHCID 23726265HCID 23726265, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

A solution of sulfur dioxide was prepared by bubbling sulfur dioxide (3.9 g, 61 mmol) in a solution of anhydrous acetonitrile (20 ml) at ambient temperature. This solution was added to PhSCF2SiMe3 (4.3 g, 18.4 mmol, obtained according to the procedure from example 6) and stirred at ambient temperature under an inert atmosphere. Anhydrous CsF (2.8 g, 18.5 mmol) was then added to the reaction mixture, which was stirred at ambient temperature overnight. The reaction was monitored by TLC and by 19F NMR (CDCl3) until the disappearance of PhSCF2SiMe3. F-TEDA (7.15 g, 20 mmol) was added to the mixture, at −20° C., which was then stirred for 1 h at ambient temperature. The mixture was concentrated and the solid residue washed with ethyl ether (10×50 ml). The filtrate was evaporated and the product purified by bulb-to-bulb distillation. The product difluoro(phenylsulfanyl)methanesulfonyl fluoride was obtained in the form of a colorless liquid (2.5 g, 57%).

Workup

  1. customobtained
  2. stirringwas stirred at ambient temperature overnight
  3. stirringwhich was then stirred for 1 h at ambient temperature
  4. concentrationThe mixture was concentrated
  5. washthe solid residue washed with ethyl ether (10×50 ml)
  6. customThe filtrate was evaporated
  7. distillationthe product purified by bulb-to-bulb distillation

Sources & evidence

ORD record
ord-4fd926c4374d4e32a57a352e63167b10
Source dataset
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08853448B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes