Acetonitrile → 4-(2-Pyridylmethyl)-2-dodecyl-2H-tetrazole

HRID 2380461Notes

Reaction equation

HRID 2380461 reaction equation
N1C=CC=CC=1C[C:8]1[NH:12][N:11]=[N:10][N:9]=1.C([N:15]([CH2:18][CH3:19])[CH2:16][CH3:17])C.Br[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].[C:33](#N)[CH3:34]>CCCCCC>[N:15]1[CH:16]=[CH:17][CH:34]=[CH:33][C:18]=1[CH2:19][N:9]1[CH:8]=[N:12][N:11]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[NH:10]1

Participants

6

Reactant 4

HCID 6342AcetonitrileHCID 8471TriethylamineHCID 89191-BromododecaneHCID 178420215HCID 178420215, compound

Product 1

HCID 214695704-(2-Pyridylmethyl)-2-dodecyl-2H-tetrazole

Reagents, catalysts & solvents 1

HCID 8058HexaneSolvent

Procedure

The tetrazole (a) (3.0 g; 0.015 moles) was taken up in acetonitrile (50 mL) containing two equivalents of triethylamine (3.0 g; 0.030 moles). The suspension was heated to reflux and then treated with 1-bromododecane (3.7 g; 0.015 moles) dropwise for several minutes. The solution was refluxed for 16 hours, cooled to room temperature, and the solvent removed in vacuo. The residue was triturated with ethyl acetate, filtered, and concentration of the filtrate in vacuo leaving a maroon-colored liquid. The 2-isomer was obtained by dissolving the crude product in 50% hexane/50% ethyl acetate and removing the impurities, including the 1-regioisomer, by silica gel chromatography. Yield: 2.0 g (41%) .

Workup

  1. temperatureThe suspension was heated
  2. temperatureto reflux
  3. temperatureThe solution was refluxed for 16 hours
  4. customthe solvent removed in vacuo
  5. customThe residue was triturated with ethyl acetate
  6. filtrationfiltered
  7. customconcentration of the filtrate in vacuo leaving a maroon-colored liquid
  8. customThe 2-isomer was obtained
  9. customremoving the impurities

Sources & evidence

ORD record
ord-10234d6a51684992b310ef2c16e8c123
Source dataset
uspto-grants-1994_11
Patent number
US05366987

Reaction notes

Loading…