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Phosphorus oxychloride → 2-Chloro-3-iodo-5-nitropyridine

HRID 42040
Notes
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Reaction equation

HRID 42040 reaction equation
[I:1][C:2]1[C:3](O)=[N:4][CH:5]=[C:6]([N+:8]([O-:10])=[O:9])[CH:7]=1.O=P(Cl)(Cl)[Cl:14].P(Cl)(Cl)(Cl)(Cl)Cl>O>[Cl:14][C:3]1[C:2]([I:1])=[CH:7][C:6]([N+:8]([O-:10])=[O:9])=[CH:5][N:4]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 178526840HCID 178526840, compound

Product 1

HCID 111406392-Chloro-3-iodo-5-nitropyridineYield 69%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
140 °C

Procedure

A mixture of 3-iodo-5-nitropyridin-2-ol (37.60 mmol, 10 g), POCl3 (86.47 mmol, 7.94 ml) and PCl5 (48.87 mmol, 10.2 g) was heated at 140° C. for 45 minutes under argon atmosphere. The mixture was cooled at room temperature, poured slowly over iced-water and extracted with dichloromethane. The organic phase was washed with water, NaHCO3 aqueous solution and brine. The solvent was evaporated and the crude mixture was purified by chromatography over SiO2 eluting hexane/DCM mixtures affording 7.32 g (yield 69%) of the expected product.

Workup

  1. temperatureThe mixture was cooled at room temperature
  2. extractionextracted with dichloromethane
  3. washThe organic phase was washed with water, NaHCO3 aqueous solution and brine
  4. customThe solvent was evaporated
  5. customthe crude mixture was purified by chromatography over SiO2
  6. washeluting hexane/DCM

Sources & evidence

ORD record
ord-b60a025c8511475d85932bcdd513b7ee
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08536165B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes