تفاعل #2146723

ord-71b842c4d18a48378a2c92fdef1c20f5

معادلة التفاعل

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
المردود 83.0%

المذيبات

ظروف التفاعل

درجة الحرارة
40°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةSubsequently, the reaction solution was cooled to room temperature (about 25° C.)
  2. 2
    أخرىwas precipitated
  3. 3
    ترشيحThis was filtered
  4. 4
    غسيلthe residue was washed with water until the pH of the filtrate
  5. 5
    أخرىThen the residue was dried under reduced pressure
  6. 6
    أخرىaffording a yellow powdery product
  7. 7
    أخرىThe product was purified by column chromatography (eluate: ethyl acetate/toluene=⅓:volume ratio)

الإجراء التجريبي

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)}.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08278030B2uspto-grants-2012_10