반응 #2146723

ord-71b842c4d18a48378a2c92fdef1c20f5

반응 방정식

OO
hydrogen peroxide
O=c1c2ccccc2sc2ccc(Sc3ccccc3)cc12
2-(phenylthio)thioxanthone
CC#N
acetonitrile
O=S(=O)(O)O
sulfuric acid
O=c1c2ccccc2sc2ccc(S(=O)c3ccccc3)cc12
2-[(phenyl)sulfinyl]thioxanthone
수율 83.0%

용매

반응 조건

온도
40°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도Subsequently, the reaction solution was cooled to room temperature (about 25° C.)
  2. 2
    기타was precipitated
  3. 3
    여과This was filtered
  4. 4
    세척the residue was washed with water until the pH of the filtrate
  5. 5
    기타Then the residue was dried under reduced pressure
  6. 6
    기타affording a yellow powdery product
  7. 7
    기타The product was purified by column chromatography (eluate: ethyl acetate/toluene=⅓:volume ratio)

실험 절차

While 11.2 parts of 2-(phenylthio)thioxanthone synthesized in Production Example 1, 215 parts of acetonitrile, and 0.02 parts of sulfuric acid were stirred at 40° C., 4.0 parts of a 30% aqueous hydrogen peroxide solution was dropped thereto slowly and then a reaction was performed at 40 to 45° C. for 14 hours. Subsequently, the reaction solution was cooled to room temperature (about 25° C.) and then was poured into 200 parts of distilled water, so that the product was precipitated. This was filtered and the residue was washed with water until the pH of the filtrate became neutral. Then the residue was dried under reduced pressure, affording a yellow powdery product. The product was purified by column chromatography (eluate: ethyl acetate/toluene=⅓:volume ratio) to afford 2-[(phenyl)sulfinyl]thioxanthone in a yield of 83%. The product was identified by 1H-NMR {d6-dimethyl sulfoxide, δ (ppm) 8.75 (1H, s), 8.45 (1H, d), 8.01 (2H, d), 7.75-7.85 (4H, m), 7.53-7.62 (4H, m)}.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08278030B2uspto-grants-2012_10