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Diethyl Ether → 2,4,6-Triiodo-1,3,5-tris-(aminoethoxymethyl)benzene

HRID 1271813
Notes
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Reaction equation

HRID 1271813 reaction equation
[I:1][C:2]1[C:7]([CH2:8][O:9][CH2:10][CH2:11][NH:12]C(OC(C)(C)C)=O)=[C:6]([I:20])[C:5]([CH2:21][O:22][CH2:23][CH2:24][NH:25]C(OC(C)(C)C)=O)=[C:4]([I:33])[C:3]=1[CH2:34][O:35][CH2:36][CH2:37][NH:38]C(OC(C)(C)C)=O.FC(F)(F)C(O)=O.C(OCC)C.[OH-].[Na+]>ClCCl.O>[I:1][C:2]1[C:3]([CH2:34][O:35][CH2:36][CH2:37][NH2:38])=[C:4]([I:33])[C:5]([CH2:21][O:22][CH2:23][CH2:24][NH2:25])=[C:6]([I:20])[C:7]=1[CH2:8][O:9][CH2:10][CH2:11][NH2:12]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 3283Diethyl Ether2×HCID 6422Trifluoroacetic acidHCID 14798Sodium HydroxideHCID 184548882,4,6-Triiodo-1,3,5-tris-(2-tert-butoxycarbonylaminoethoxymethyl)benzene

Product 1

HCID 865956492,4,6-Triiodo-1,3,5-tris-(aminoethoxymethyl)benzene

Reagents, catalysts & solvents 2

HCID 962
Water
Solvent
HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
0 °C

Procedure

24.4 g (25 mmol) of 2,4,6-triiodo-1,3,5-tris-(2-tert-butoxycarbonylaminoethoxymethyl)benzene is dissolved in 100 ml of dichloromethane, mixed at 0° C. with 100 ml of trifluoroacetic acid and stirred for 3 hours at 0° C. The batch is poured into 500 ml of diethyl ether, the solid that accumulates in this case is suctioned off and rewashed several times with diethyl ether. The residue is dissolved in 100 ml of water and 100 ml of dichloromethane while being stirred vigorously, and 32% NaOH solution is added until a pH of 10 is reached. The organic phase is separated, the aqueous phase is extracted three times with 50 ml each of dichloromethane, the combined organic phases are dried on magnesium sulfate and evaporated to the dry state.

Workup

  1. customThe organic phase is separated
  2. extractionthe aqueous phase is extracted three times with 50 ml each of dichloromethane
  3. customthe combined organic phases are dried on magnesium sulfate
  4. customevaporated to the dry state

Sources & evidence

ORD record
ord-2a0584e5107a4ab896d189fb059aa205
Source dataset
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07208140B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes