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Water → Diethylenetriaminepentaacetic acid

HRID 1534086
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HRID 1534086 반응식
N1CC[O:4]CC1.[CH2:7]1[N:14]([CH2:15][CH2:16][NH+:17]([CH2:28][C:29]([O-:31])=[O:30])[CH2:18][CH2:19][N:20]2[CH2:27][C:25](=[O:26])[O:24][C:22](=[O:23])[CH2:21]2)[CH2:13][C:11](=[O:12])[O:10][C:8]1=[O:9].[OH2:32]>>[CH2:16]([N:17]([CH2:28][C:29]([OH:31])=[O:30])[CH2:18][CH2:19][N:20]([CH2:27][C:25]([OH:26])=[O:4])[CH2:21][C:22]([OH:24])=[O:23])[CH2:15][N:14]([CH2:7][C:8]([OH:10])=[O:9])[CH2:13][C:11]([OH:12])=[O:32]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 962WaterHCID 8083MorpholineHCID 16760401Diethylenetriaminepentaacetic dianhydride

생성물 1

HCID 3053Diethylenetriaminepentaacetic acid

실험 절차

To a 2-liter round bottom flask containing morpholine (400 mL, 4.60 mol) was added DTPA dianhydride (71.5 g, 200 mmol) followed by 150 mL of water. The reaction was stirred for 24 hours and concentrated. The crude material was evaporated three times from 400 mL water and then stirred with 1 L of dry ethanol at 50° C. for 18 hours. The suspension was filtered and the solids were purified by ion-exchange chromatography on AGl-X8 (hydroxide form) resin eluting with water followed by 0.2 N acetic acid to afford 53.0 g of DTPA-BMO.

후처리

  1. concentration
concentrated
  • customThe crude material was evaporated three times from 400 mL water
  • stirringstirred with 1 L of dry ethanol at 50° C. for 18 hours
  • filtrationThe suspension was filtered
  • customthe solids were purified by ion-exchange chromatography on AGl-X8 (hydroxide form) resin
  • washeluting with water
  • 출처 및 근거

    ORD 기록
    ord-dda112e2f3ce4f509f5ab04d3677feee
    출처 데이터셋
    uspto-grants-1992_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05087440

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