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N-Iodosuccinimide → 1-(5-Chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone

HRID 626827
Notes
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Reaction equation

HRID 626827 reaction equation
[Cl:1][C:2]1[C:3]([F:12])=[CH:4][C:5]([OH:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1.[I:13]N1C(=O)CCC1=O>C(O)(=O)C>[Cl:1][C:2]1[C:3]([F:12])=[C:4]([I:13])[C:5]([OH:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 120273N-IodosuccinimideHCID 162214361-(5-Chloro-4-fluoro-2-hydroxyphenyl)ethanone

Product 1

HCID 866668571-(5-Chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
70 °C

Procedure

A solution of 1-(5-chloro-4-fluoro-2-hydroxyphenyl)ethanone (23.8 g, 126 mmol) in acetic acid (100 mL) was treated with N-iodosuccinimide (34.1 g, 151 mmol) and stirred at 70° C. for 2 hr. The reaction mixture was concentrated, diluted with EtOAc and quenched with sat. NaHCO3 solution until the bubbling stopped. The organic layers were separated, washed with water, dried over MgSO4 and stripped to give the desired product which was used in the next step without further purification.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with EtOAc
  3. customquenched with sat. NaHCO3 solution until the bubbling
  4. customThe organic layers were separated
  5. washwashed with water
  6. dry with materialdried over MgSO4

Sources & evidence

ORD record
ord-739c2e1325ec4b5cbca0537fbcea6110
Source dataset
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09309251B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes