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Pyridine → 1,3,5-Triiodobenzene-2,4,6-trialdehyde

HRID 1418257
Notes
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Reaction equation

HRID 1418257 reaction equation
[I:1][C:2]1[C:7]([CH2:8][OH:9])=[C:6]([I:10])[C:5]([CH2:11][OH:12])=[C:4]([I:13])[C:3]=1[CH2:14][OH:15].C(N(CC)CC)C.N1C=CC=CC=1>CS(C)=O>[I:1][C:2]1[C:3]([CH:14]=[O:15])=[C:4]([I:13])[C:5]([CH:11]=[O:12])=[C:6]([I:10])[C:7]=1[CH:8]=[O:9]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 1049PyridineHCID 8471TriethylamineHCID 206936271,3,5-Triiodo-2,4,6-trihydroxymethylbenzene

Product 1

HCID 184293191,3,5-Triiodobenzene-2,4,6-trialdehyde

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Conditions

Temperature
0 °C

Procedure

1,3,5-Triiodo-2,4,6-trihydroxymethylbenzene (4.5 g, 8.2 mmol) was dissolved in DMSO (80 ml). Triethylamine (51.7 ml, 371 mmol) and pyridine.SO3 (11.8 g, 74.2 mmol) were added and the mixture was stirred for two hours. The two phases were separated and the lower phase was cooled to 0° C., poured into water (150 ml) and stirred for 30 min at 0° C. The white solid was collected by filtration, washed with water and dried. Yield: 3.0 g (67%).

Workup

  1. additionSO3 (11.8 g, 74.2 mmol) were added
  2. customThe two phases were separated
  3. additionpoured into water (150 ml)
  4. stirringstirred for 30 min at 0° C
  5. filtrationThe white solid was collected by filtration
  6. washwashed with water
  7. customdried

Sources & evidence

ORD record
ord-bfed357575d64ceebe141e406e37ff24
Source dataset
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05882628

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes