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Diethylenetriaminepentaacetic acid → DTPA dianhydride

HRID 41801
Notes
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Reaction equation

HRID 41801 reaction equation
[CH2:1]([N:12]([CH2:24][C:25]([OH:27])=[O:26])[CH2:13][CH2:14][N:15]([CH2:20][C:21]([OH:23])=O)[CH2:16][C:17]([OH:19])=[O:18])[CH2:2][N:3]([CH2:8][C:9]([OH:11])=[O:10])[CH2:4][C:5]([OH:7])=O.C(OC(=O)C)(=O)C>N1C=CC=CC=1>[CH2:20]1[N:15]([CH2:14][CH2:13][N:12]([CH2:24][C:25]([OH:27])=[O:26])[CH2:1][CH2:2][N:3]2[CH2:8][C:9](=[O:10])[O:11][C:5](=[O:7])[CH2:4]2)[CH2:16][C:17](=[O:19])[O:18][C:21]1=[O:23]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 3053Diethylenetriaminepentaacetic acidHCID 7918Acetic Anhydride

Product 1

HCID 100825DTPA dianhydride

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

1.08 gram of DTPA (2.7 mmol), 2 mL acetic anhydride and 1.3 mL pyridine were stirred for 48 hours at 60° C. and then the reaction mixture was filtered at room temperature. The solid product washed to be free of pyridine with acetic anhydride and then with diethyl ether, and is dried.

Workup

filtration
the reaction mixture was filtered at room temperature
  • washThe solid product washed
  • dry with materialwith diethyl ether, and is dried
  • Sources & evidence

    ORD record
    ord-c95a531273a7400eacd53b7c1e81426f
    Source dataset
    uspto-grants-2013_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08532742B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes