4-(1-Azidotridecyl)-2-triethylsilylfuran → 4-(1-Aminotridecyl)-2-triethylsilylfuran

HRID 488218Notes

Reaction equation

HRID 488218 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[N:7]([CH:10]([C:23]1[CH:24]=[C:25]([Si:28]([CH2:33][CH3:34])([CH2:31][CH3:32])[CH2:29][CH3:30])[O:26][CH:27]=1)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])=[N+]=[N-]>C1COCC1>[NH2:7][CH:10]([C:23]1[CH:24]=[C:25]([Si:28]([CH2:33][CH3:34])([CH2:31][CH3:32])[CH2:29][CH3:30])[O:26][CH:27]=1)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]

Participants

4

Procedure

A solution of lithium aluminum hydride (a 1.0 M solution in THF; 4.22 ml, 4.22 mmol) was added slowly to a solution of 4-(1-azidotridecyl)-2-triethylsilylfuran (1.55 g, 3.84 mmol) at 0 degrees C under argon. After stirring at room temperature for 2 hours, the mixture was cooled to 0 degrees C. and quenched with 2M sodium hydroxide. Anhydrous sodium sulfate was added to coagulate the aluminum salt and the mixture was extracted thoroughly with ethyl acetate. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 5% methanol/dichloromethane to give the titled amine.

Workup

  1. temperaturethe mixture was cooled to 0 degrees C
  2. customand quenched with 2M sodium hydroxide
  3. additionAnhydrous sodium sulfate was added
  4. extractionthe mixture was extracted thoroughly with ethyl acetate
  5. customEvaporation of the
  6. dry with materialdried (magnesium sulfate)
  7. customextracts gave an oil, which
  8. customwas purified by flash chromatography on silica using 5% methanol/dichloromethane

Sources & evidence

ORD record
ord-87f3af29eb3d4f92b9c172505877c7fb
Source dataset
uspto-grants-1994_03
Patent number
US05298633

Reaction notes

Loading…