Bromocyclopentane → 3-(Cyclopentyloxy)-4-methoxyaniline

HRID 1584969Notes

Reaction equation

HRID 1584969 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([OH:8])[CH:7]=1.[H-].[Na+].[CH:13]1(Br)[CH2:17][CH2:16][CH2:15][CH2:14]1>O1CCOCC1.CN(C)C=O.[I-].[K+]>[CH:13]1([O:8][C:6]2[CH:7]=[C:2]([CH:3]=[CH:4][C:5]=2[O:9][CH3:10])[NH2:1])[CH2:17][CH2:16][CH2:15][CH2:14]1

Participants

7

Conditions

Temperature
60 °C

Procedure

A stirred solution of 5-amino-2-methoxyphenol (10 g) in dry dioxane (150 mL) is treated portionwise with an oil suspension of sodium hydride (60%; 3 g; 75 mmol) and the mixture is then warmed at 60° C. for 30 minutes. It is then treated dropwise with a solution of cyclopentyl bromide (9.2 mL) and potassium iodide (50 mg) in dry dimethylformamide (20 mL) and heated at reflux for 5 hours. The mixture is then concentrated and the residue is treated with ethyl acetate (200 mL) and water (200 mL). The organic layer is then separated, washed with water (100 mL), aqueous sodium hydroxide solution (250 mL;1N), and with water (100 mL), and dried over magnesium sulfate. The concentration of the reaction mixture gives a dark oil, which is subjected to flash chromatography, eluting with a mixture of n-hexane and ethyl acetate (1:1 v/v), to give 3-cyclopentyloxy-4-methoxyaniline (4.43 g), in the form of an oil.

Workup

  1. temperatureheated
  2. temperatureat reflux for 5 hours
  3. concentrationThe mixture is then concentrated
  4. additionthe residue is treated with ethyl acetate (200 mL) and water (200 mL)
  5. customThe organic layer is then separated
  6. washwashed with water (100 mL), aqueous sodium hydroxide solution (250 mL;1N)
  7. dry with materialwith water (100 mL), and dried over magnesium sulfate
  8. customThe concentration of the reaction mixture gives a dark oil, which
  9. washeluting with a mixture of n-hexane and ethyl acetate (1:1 v/v)

Sources & evidence

ORD record
ord-3c5375534f4d4da79043f859e3218398
Source dataset
uspto-grants-1999_08
Patent number
US05935978

Reaction notes

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