Sodium 4-cyanobenzenesulfinate → 3-Ethyl-2-methylbenzoxazolium 4-Cyanobenzenesulfinate

HRID 1829858Notes

Reaction equation

HRID 1829858 reaction equation
[Cl-].[CH2:2]([N+:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]=1[CH3:13])[CH3:3].[C:14]([C:16]1[CH:21]=[CH:20][C:19]([S:22]([O-:24])=[O:23])=[CH:18][CH:17]=1)#[N:15].[Na+]>C(O)C>[C:14]([C:16]1[CH:17]=[CH:18][C:19]([S:22]([O-:24])=[O:23])=[CH:20][CH:21]=1)#[N:15].[CH2:2]([N+:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]=1[CH3:13])[CH3:3]

Participants

4

Reactant 2

HCID 23668300Sodium 4-cyanobenzenesulfinateHCID 67174878HCID 67174878, compound

Product 1

HCID 220550573-Ethyl-2-methylbenzoxazolium 4-CyanobenzenesulfinateYield 46.1%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

A solution of 3-ethyl-2-methylbenzoxazolium chloride (0.73 g) in ethanol (20 mL) was added to an Erlenmeyer flask containing a magnetically stirred boiling solution of sodium 4-cyanobenzenesulfinate (0.1 g) in anhydrous ethanol (20 mL). The mixture was allowed to cool to room temperature and was then further cooled in an ice bath. The mixture was filtered and the filtrate was concentrated to dryness using a rotary evaporator. The residue was mixed with deionized water and this mixture was extracted with ethyl acetate (2×20 mL). The combined organic extracts were concentrated to dryness using a rotary evaporator. The resultant solid was then dissolved in methylene chloride, filtered and evaporated to dryness using a rotary evaporator to afford 0.08 g of product.

Workup

  1. additioncontaining
  2. temperaturewas then further cooled in an ice bath
  3. filtrationThe mixture was filtered
  4. concentrationthe filtrate was concentrated to dryness
  5. customa rotary evaporator
  6. additionThe residue was mixed with deionized water
  7. extractionthis mixture was extracted with ethyl acetate (2×20 mL)
  8. concentrationThe combined organic extracts were concentrated to dryness
  9. customa rotary evaporator
  10. dissolutionThe resultant solid was then dissolved in methylene chloride
  11. filtrationfiltered
  12. customevaporated to dryness
  13. customa rotary evaporator

Sources & evidence

ORD record
ord-7f6e1045315a4d8a8b84dde7b2d9e5d5
Source dataset
uspto-grants-2006_06
Patent number
US07064152B2

Reaction notes

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