Benzyl Bromide → 2-ethyl-5-methoxy-1-(phenylmethyl)-1H-indole

HRID 566685Notes

Reaction equation

HRID 566685 reaction equation
[CH2:1]([C:3]1[NH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([O:12][CH3:13])=[CH:7][CH:6]=2)[CH3:2].C1COCC1.[H-].[Na+].[CH2:21](Br)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>CN(C=O)C.O>[CH2:1]([C:3]1[N:4]([CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([O:12][CH3:13])=[CH:7][CH:6]=2)[CH3:2]

Participants

7

Reactant 4

HCID 7498Benzyl BromideHCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 107024052-ethyl-5-methoxy-1H-indole

Product 1

HCID 105158362-ethyl-5-methoxy-1-(phenylmethyl)-1H-indoleYield 82%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

2-Ethyl-5-methoxy-1H-indole (5.6 g, 21.5 mmol) was dissolved in 150 mL of DMF and 20 mL of THF and 1.0 g (25 mmol) of 60% sodium hydride was added. After stirring for 0.17 hours, 3.0 mL (25 mmol) of benzyl bromide was added. The mixture was stirred at room temperature for 10 hours, diluted with water and extracted with ethyl acetate. The ethyl acetate solution was washed with water, saturated NaCl solution, and dried (Na2SO4). The EtOAc was evaporated and the residue was chromatographed on silica gel eluting with a gradient, 5% EtOAc/hexane→15% EtOAc/hexane to give 4.6 g (82% yield) of 2-ethyl-5-methoxy-1-(phenylmethyl)-1H-indole.

Workup

  1. stirringThe mixture was stirred at room temperature for 10 hours
  2. extractionextracted with ethyl acetate
  3. washThe ethyl acetate solution was washed with water, saturated NaCl solution
  4. dry with materialdried (Na2SO4)
  5. customThe EtOAc was evaporated
  6. customthe residue was chromatographed on silica gel eluting with a gradient, 5% EtOAc/hexane→15% EtOAc/hexane

Sources & evidence

ORD record
ord-a622df7959a9472d94a087219e1b9f1e
Source dataset
uspto-grants-2001_01
Patent number
US06175021B1

Reaction notes

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