반응 #1375815

ord-a38a23bfc67943b0ab8dd6e927b402ff

반응 방정식

COCC1CO1
glycidyl methyl ether
O=C(O)CN1CCNCCN(CC(=O)O)CCN(CC(=O)O)CC1
1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane
[K+].[OH-]
potassium hydroxide
COCC(O)CN1CCN(CC(=O)O)CCN(CC(=O)O)CCN(CC(=O)O)CC1
10-(2-Hydroxy-3-methoxy-propyl)-1,4,7-tris-carboxymethyl-1,4,7,10-tetraazacyclododecane

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타It is evaporated to dryness
  2. 2
    추출extracted twice with 100 ml of tert-butyl methyl ether
  3. 3
    기타evaporated to dryness
  4. 4
    추출(extracted) with 200 ml of methanol/80 ml of methylene chloride
  5. 5
    온도It is cooled in an ice bath
  6. 6
    기타precipitated potassium chloride
  7. 7
    여과is filtered out
  8. 8
    농축The 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
    세척The product is eluted with a solution of ethanol/water 1:3
  11. 11
    농축After concentration
  12. 12
    기타by evaporation in a vacuum
  13. 13
    기타the residue is chromatographed on a reversed-phase column (RP 18/mobile solvent =gradient of water/tetrahydrofuran)
  14. 14
    농축After concentration
  15. 15
    기타by evaporation of the main fraction, 10.38 g (77% of theory) of a greatly hygroscopic, vitreous solid
  16. 16
    기타is obtained

실험 절차

7.63 g (86.58 mmol) of glycidyl methyl ether and 10 g (28.86 mmol) of 1,4,7-triscarboxymethyl-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 50° 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 (77% of theory) of a greatly hygroscopic, vitreous solid is obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05747000uspto-grants-1998_05