Isopropyl iodide → HCID 22930520, compound

HRID 1435751Notes

Reaction equation

HRID 1435751 reaction equation
I[CH:2]([CH3:4])[CH3:3].[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([OH:16])=[C:10]([CH:15]=1)[C:11]([O:13][CH3:14])=[O:12].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([O:16][CH:2]([CH3:4])[CH3:3])=[C:10]([CH:15]=1)[C:11]([O:13][CH3:14])=[O:12]

Participants

5

Procedure

A mixture of 2-iodo-propane (2.2 ml, 22 mmol), methyl 5-chloro-2-hydroxy-benzoate (2.0 g, 10.7 mmol), potassium carbonate (3.0 g, 10.9 mmol), and acetonitrile (40 ml) was heated under reflux for 3 hours. After cooling to room temperature, the mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was partitioned between ethyl acetate (100 ml) and saturated aqueous sodium chloride solution (100 ml). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with dichloromethane-hexane (1:3 followed by 1:2 followed by 1:1) to provide methyl 5-chloro-2-isopropoxy-benzoate (1.2 g, 49% yield).

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 3 hours
  3. filtrationthe mixture was filtered
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customThe residue was partitioned between ethyl acetate (100 ml) and saturated aqueous sodium chloride solution (100 ml)
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by flash chromatography on silica gel eluting with dichloromethane-hexane (1:3 followed by 1:2 followed by 1:1)

Sources & evidence

ORD record
ord-885b17d8d0a8401b9e06585cfa4bffed
Source dataset
uspto-grants-2009_11
Patent number
US07618968B2

Reaction notes

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