تفاعل #1929019

ord-2caf0f77d101431bafcd0a432140584f

معادلة التفاعل

Cc1ccc(S(=O)(=O)N2CCN(S(=O)(=O)c3ccc(C)cc3)CCN(S(=O)(=O)c3ccc(C)cc3)CC2)cc1
1,4,7-Tris(p-toluenesulfonyl)-1,4,7-triazacyclononane
Oc1ccccc1
phenol
Cc1ccc(S(=O)(=O)N2CCNCCNCC2)cc1
1-(p-toluenesulfonyl)-1,4,7-triazacyclononane
المردود 88.0%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter returning to ambient temperature
  2. 2
    ترشيحthe mixture is filtered
  3. 3
    غسيلthe solid is washed with diethyl ether (2×80 ml)
  4. 4
    workup.DISSOLUTIONThe hydrobromide salt is dissolved in a 1M sodium hydroxide solution until the pH
  5. 5
    استخلاصThe aqueous solution is extracted with chloroform (8×50 ml)
  6. 6
    تجفيفThe combined organic phases are dried over Na2SO4
  7. 7
    أخرىthe solvent is evaporated under vacuum
  8. 8
    أخرىFinally, a white solid is obtained (7.36 g, yield 88%)

الإجراء التجريبي

1,4,7-Tris(p-toluenesulfonyl)-1,4,7-triazacyclononane (17.56 g, 29.7 mmol) and phenol (21 g, 223.0 mmol) are dissolved in 240 ml of a solution of HBr (33%) in glacial acetic acid. The solution is heated at 90° C. for 30 h. A solid appears after 3 h. After returning to ambient temperature, the mixture is filtered and the solid is washed with diethyl ether (2×80 ml). The hydrobromide salt is dissolved in a 1M sodium hydroxide solution until the pH is of the order of 12 units. The aqueous solution is extracted with chloroform (8×50 ml). The combined organic phases are dried over Na2SO4 and the solvent is evaporated under vacuum. Finally, a white solid is obtained (7.36 g, yield 88%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08945514B2uspto-grants-2015_02