Ethyl 4-iodobenzoate → Ethyl 4-cyclopropylbenzoate

HRID 1351531Notes

Reaction equation

HRID 1351531 reaction equation
[Cl-].[Cl-].[Cl-].[In+3].[CH:5]1([Mg]Br)[CH2:7][CH2:6]1.[CH2:10]([O:12][C:13](=[O:21])[C:14]1[CH:19]=[CH:18][C:17](I)=[CH:16][CH:15]=1)[CH3:11]>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[CH2:10]([O:12][C:13](=[O:21])[C:14]1[CH:19]=[CH:18][C:17]([CH:5]2[CH2:7][CH2:6]2)=[CH:16][CH:15]=1)[CH3:11]

Participants

6

Conditions

Temperature
-70 °C

Procedure

Indium trichloride (2.2 g, 10 mmol) and THF (50 mL) were combined under nitrogen and cooled to −70° C. Cyclopropylmagnesium bromide solution (33 mL, 30 mmol, 0.92 M) was added dropwise while maintaining the reaction temperature ≦−60° C. After the addition was complete, the reaction was stirred 0.5 h with cooling then 0.5 h with the cooling bath removed. The resulting solution was added via cannula to a refluxing solution of ethyl-4-iodobenzoate (5.5 g, 20 mmol), trans-dichlorobis(triphenylphosphine)palladium(II) (421 mg, 0.60 mmol) and THF (100 mL) under nitrogen. After 24 h, the contents of the reaction flask were cooled and the solvent was removed in vacuo. Water (100 mL) and 5% KHSO4 were added and the mixture was extracted with CH2Cl2 (3×100 mL). The combined organic extracts were washed with brine, dried with Na2SO4 and filtered. The filtrate was removed in vacuo and the remaining residue was purified by flash column chromatography (hexane:EtOAc 95:5) to give 4cyclopropyl-benzoic acid ethyl ester as an orange oil.

Workup

  1. temperaturewhile maintaining the reaction temperature ≦−60° C
  2. additionAfter the addition
  3. temperaturewith cooling
  4. custom0.5 h with the cooling bath removed
  5. waitAfter 24 h
  6. temperaturethe contents of the reaction flask were cooled
  7. customthe solvent was removed in vacuo
  8. additionWater (100 mL) and 5% KHSO4 were added
  9. extractionthe mixture was extracted with CH2Cl2 (3×100 mL)
  10. washThe combined organic extracts were washed with brine
  11. dry with materialdried with Na2SO4
  12. filtrationfiltered
  13. customThe filtrate was removed in vacuo
  14. customthe remaining residue was purified by flash column chromatography (hexane:EtOAc 95:5)

Sources & evidence

ORD record
ord-f5c69b7fb41f4dc4a671bff1113898e2
Source dataset
uspto-grants-2007_05
Patent number
US07217716B2

Reaction notes

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