تفاعل #1375819

ord-3a81dd53a92846998e786ccbc502db7c

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزIt is concentrated by evaporation in a vacuum
  2. 2
    workup.DISSOLUTIONthe residue is dissolved in 100 ml of water
  3. 3
    workup.ADDITIONby adding 12 N hydrochloric acid
  4. 4
    غسيلIt is eluted with 2 l of water, which
  5. 5
    تركيزThis solution is concentrated by evaporation in a vacuum
  6. 6
    workup.DISSOLUTIONthe residue is dissolved in 100 ml of water
  7. 7
    workup.ADDITIONenough cation exchanger IR-120 is added in portions up to pH 3.5
  8. 8
    ترشيحThe solution is filtered
  9. 9
    أخرىfreeze-dried

الإجراء التجريبي

5 g (14.43 mmol) of 1,4,7-tris-(carboxymethyl)-1,4,7, 10-tetraazacyclododecane is stirred in 75 ml of dimethylformamide for 18 hours with 3.14 g (17.35 mmol) of (2-bromoethyl)-tert-butyl ether and 6.50 g of potassium carbonate at 95° C. It is concentrated by evaporation in a vacuum and the residue is dissolved in 100 ml of water, the pH is adjusted to 2 by adding 12 N hydrochloric acid and the solution is put on a column of 320 ml of cation exchanger IR-120 (H+ form). It is eluted with 2 l of water, which is discarded, then with 2 l of 0.5 N ammonia solution. This solution is concentrated by evaporation in a vacuum, the residue is dissolved in 100 ml of water. With stirring, enough cation exchanger IR-120 is added in portions up to pH 3.5. The solution is filtered and freeze-dried and 4.19 g of the title compound is obtained as white solid with a water content of 6.3%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05747000uspto-grants-1998_05