Hydrochloric Acid → 7-Bromo-2-methyl-1-benzofuran

HRID 2355517Notes

Reaction equation

HRID 2355517 reaction equation
[Br:1][C:2]1[C:10]2[O:9][CH:8]=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Li+].[CH3:12]C([N-]C(C)C)C.C1COCC1.CCCCCCC.CI.Cl>C1COCC1>[Br:1][C:2]1[C:10]2[O:9][C:8]([CH3:12])=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1

Participants

7

Conditions

Temperature
-70 °C

Procedure

A stirred solution of 7-bromobenzofuran (493 mg, 2.5 mmol) in dry THF (5 mL) was cooled to −70° C. and 2M LDA in 1:1 THF/heptane (1.4 mL, 2.8 mmol) was added dropwise over 2 min. The mixture was stirred at −70° C. for 1 h and methyl iodide (0.19 mL, 3.0 mmol) was added. The mixture was stirred at −70° C. for 3 h and at 0° C. for 1 h. The mixture was poured into 5% aq HCl (60 mL) and extracted with ether (2×50 mL). The combined ether extracts were washed with sat'd aq NaHCO3 (20 mL) and dried over MgSO4. Removal of the solvent left an oil (470 mg) which was purified by chromatography on a 40-g silica cartridge eluted with hexanes to afford 7-bromo-2-methylbenzofuran (277 mg, 52%, estimated purity 80%).

Workup

  1. stirringThe mixture was stirred at −70° C. for 3 h and at 0° C. for 1 h
  2. extractionextracted with ether (2×50 mL)
  3. washThe combined ether extracts were washed with sat'd aq NaHCO3 (20 mL)
  4. dry with materialdried over MgSO4
  5. customRemoval of the solvent
  6. waitleft an oil (470 mg) which
  7. customwas purified by chromatography on a 40-g silica cartridge
  8. washeluted with hexanes

Sources & evidence

ORD record
ord-9a39fbee365b4639aa6843a0305d7096
Source dataset
uspto-grants-2010_07
Patent number
US07754737B2

Reaction notes

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