تفاعل #1375816

ord-4829568d8adb4b4b92574ae20dd14bae

معادلة التفاعل

CC(C)(C)OCC1CO1
glycidyl-tert-butyl ether
O=C(O)CN1CCNCCN(CC(=O)O)CCN(CC(=O)O)CC1
1,4,7-tris-carboxymethyl-1,4,7,10-tetraazacyclododecane
[K+].[OH-]
potassium hydroxide
CC(C)(C)OCC(O)CN1CCN(CC(=O)O)CCN(CC(=O)O)CCN(CC(=O)O)CC1
10-(2-Hydroxy-3-tert-butyloxy-propyl)-1,4,7-tris-carboxymethyl-1,4,7,10-tetraazacyclododecane

المذيبات

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىIt is evaporated to dryness
  2. 2
    استخلاصextracted twice with 100 ml of tert-butyl-methyl ether
  3. 3
    أخرىevaporated to dryness
  4. 4
    استخلاص(extracted) with 200 ml of methanol/80 ml of methylene chloride
  5. 5
    درجة الحرارةIt is cooled in an ice bath
  6. 6
    أخرىprecipitated potassium chloride
  7. 7
    ترشيحis filtered out
  8. 8
    تركيزThe filtrate is concentrated by evaporation in a vacuum
  9. 9
    workup.DISSOLUTIONthe residue is dissolved in 45 ml of water/20 ml of ethanol
  10. 10
    غسيلThe product is eluted with a solution of ethanol/water 1:3
  11. 11
    تركيزAfter concentration
  12. 12
    أخرىby evaporation in a vacuum
  13. 13
    أخرىthe residue is chromatographed on a reversed-phase column (RP 18/mobile solvent =gradient of water/tetrahydrofuran)
  14. 14
    تركيزAfter concentration
  15. 15
    أخرىby evaporation of the main fraction, 10.38 g (71% of theory) of a strongly hygroscopic, vitreous solid
  16. 16
    أخرىis obtained

الإجراء التجريبي

11.27 g (86.58 mmol) of glycidyl-tert-butyl ether and 10 g (28.86 mmol) of 1,4,7-tris-carboxymethyl-1,4,7,10-tetraazacyclododecane are dissolved in a mixture of 50 ml of dioxane/80 ml of water, and the pH is brought to 10 with 6 N potassium hydroxide solution. It is stirred for 24 hours at 70° C. It is evaporated to dryness, the residue is taken up with 300 ml of water/50 ml of methanol and extracted twice with 100 ml of tert-butyl-methyl ether. The aqueous solution is adjusted to pH 1 with 5 N hydrochloric acid and evaporated to dryness. The residue is boiled out (extracted) with 200 ml of methanol/80 ml of methylene chloride. It is cooled in an ice bath and precipitated potassium chloride is filtered out. The filtrate is concentrated by evaporation in a vacuum, the residue is dissolved in 45 ml of water/20 ml of ethanol and then put on a column of poly-(4-vinylpyridine). The product is eluted with a solution of ethanol/water 1:3. After concentration by evaporation in a vacuum, the residue is chromatographed on a reversed-phase column (RP 18/mobile solvent =gradient of water/tetrahydrofuran). After concentration by evaporation of the main fraction, 10.38 g (71% of theory) of a strongly hygroscopic, vitreous solid is obtained.

المصدر

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