Methyl 4-bromobenzoate → HCID 23290991, compound

HRID 1938767Notes

Reaction equation

HRID 1938767 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH:5]=[CH2:6].Br[C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=1>C1COCC1.[Zn+2].[Br-].[Br-]>[CH2:2]([C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=1)[CH2:3][CH2:4][CH:5]=[CH2:6]

Participants

5

Conditions

Temperature
56 °C

Procedure

A mixture of dry Mg (900 mg, 37 mmol) and ZnBr2 (5.63 g, 25 mmol) in THF (25 mL) was treated with 5-bromopent-1-ene (4.45 mL, 37.6 mmol) and the subsequent suspension was heated at 56° C. for 18 h. The mixture was cooled to room temperature and methyl 4-bromobenzoate (7.1 g, 33 mmol) and tetrakis-(triphenylphosphine)palladium(0) (1.0 g, 0.865 mmol) were added, and the mixture was stirred at room temperature for 24 h. The mixture was quenched with 3N HCl (aqueous) and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous MgSO4 and evaporated at reduced pressure. The residue was purified by flash chromatography (silica gel, 5% ethyl acetate/hexane) to give the crude title compound which was used without further purification.

Workup

  1. temperatureThe mixture was cooled to room temperature
  2. customThe mixture was quenched with 3N HCl (aqueous)
  3. extractionextracted with ethyl acetate
  4. dry with materialThe combined organic extracts were dried over anhydrous MgSO4
  5. customevaporated at reduced pressure
  6. customThe residue was purified by flash chromatography (silica gel, 5% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-6e5ec2394e2d4a3a9b8d293dc48e3bef
Source dataset
uspto-grants-1997_12
Patent number
US05693636

Reaction notes

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