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

HRID 1829858노트

반응식

HRID 1829858 반응식
[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]

참가 물질

4

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-7f6e1045315a4d8a8b84dde7b2d9e5d5
출처 데이터셋
uspto-grants-2006_06
특허 번호
US07064152B2

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