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Acetonitrile → Ethyl 3-chloro-4-iodo-5-methoxybenzoate

HRID 41240
Notes
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Reaction equation

HRID 41240 reaction equation
N[C:2]1[C:12]([O:13][CH3:14])=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][C:3]=1[Cl:15].C(#N)C.[I:19]CI.N(OCCC(C)C)=O>CCCCCCC.C(OCC)(=O)C>[Cl:15][C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([O:13][CH3:14])[C:2]=1[I:19])[C:6]([O:8][CH2:9][CH3:10])=[O:7]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 6342AcetonitrileHCID 6346DiiodomethaneHCID 8053Isoamyl NitriteHCID 57912463Ethyl 4-amino-3-chloro-5-methoxybenzoate

Product 1

HCID 57912451Ethyl 3-chloro-4-iodo-5-methoxybenzoateYield 66.6%

Reagents, catalysts & solvents 1

HCID 21899848
Ethylacetate heptane
Solvent

Conditions

Temperature
70 °C

Procedure

To ethyl 4-amino-3-chloro-5-methoxybenzoate (15.8 g, 68.8 mmol), were added acetonitrile (40 mL) and diiodomethane (22.2 mL, 275 mmol) in this order, and the mixture was stirred at 70° C., and then isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise thereto over 10 minutes. The mixture was stirred at 70° C. for 40 minutes. The mixture was returned to room temperature, the solvent was then distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=8/1 then 5/1) to obtain the title compound (15.6 g, 45.8 mmol)

Workup

  1. stirringThe mixture was stirred at 70° C. for 40 minutes
  2. customwas returned to room temperature
  3. distillationthe solvent was then distilled off under reduced pressure
  4. customthe residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate

Sources & evidence

ORD record
ord-02496be81bb3406ea0711670738f8315
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08530504B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes