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Potassium Iodide → Methyl 4-(2-iodoethyl)benzoate

HRID 1015927
Notes
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Reaction equation

HRID 1015927 reaction equation
Cl[CH2:2][CH2:3][C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=1.[I-:14].[K+]>C(#N)C>[I:14][CH2:2][CH2:3][C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4875Potassium IodideHCID 22098587Methyl 4-(2-chloroethyl)benzoate

Product 1

HCID 22639144Methyl 4-(2-iodoethyl)benzoate

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

70 g (352.4 mmol) of methyl 4-(2-chloroethyl)benzoate [CAS Reg. No. 65787-72-6] and 146.2 g (880.9 mmol) of potassium iodide are suspended in 800 ml of acetonitrile and stirred under reflux for three days. After the reaction has gone to completion, the reaction solution is cooled and filtered and the filtrate is evaporated to dryness under reduced pressure. The resulting residue is purified by flash chromatography on silica gel (mobile phase:petroleum ether/ethyl acetate 30:1→20:1). This gives 101 g (348.3 mmol, 98.8% of theory) of a yellowish oil.

Workup

  1. temperatureunder reflux for three days
  2. temperaturethe reaction solution is cooled
  3. filtrationfiltered
  4. customthe filtrate is evaporated to dryness under reduced pressure
  5. customThe resulting residue is purified by flash chromatography on silica gel (mobile phase:petroleum ether/ethyl acetate 30:1→20:1)

Sources & evidence

ORD record
ord-4123fdff077a42cc9b62e0b98b8b78df
Source dataset
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07985876B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes