Aluminium lithium hydride → HCID 131714671, compound

HRID 2232254Notes

Reaction equation

HRID 2232254 reaction equation
[N:1]([CH2:4][CH2:5][CH2:6][O:7][C:8]12[CH:23]=[CH:22][CH:21]=[CH:20][CH:9]1[CH2:10][CH:11]2[C:12]([N:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)=O)=[N+]=[N-].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1.CCOCC>[NH2:1][CH2:4][CH2:5][CH2:6][O:7][C:8]12[CH:23]=[CH:22][CH:21]=[CH:20][CH:9]1[CH2:10][CH:11]2[CH2:12][N:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1

Participants

5

Procedure

A solution of the azidobenzocyclobutenylamide compound of Step 2. above (3.2 g) in THF (20.4 ml) is added dropwise to a suspension of LAH (0.93 g) in anhydrous ether (122 ml) stirred under nitrogen maintained at ice bath temperatures. The reaction mixture is refluxed for 15 hours, cooled and quenched with water (0.93 ml), aqueous sodium hydroxide (15% solution, 0.93 ml) and water (2.79 ml) and filtered. The solid is washed with ether and the combined filtrate dried, filtered, evaporated in vacuo and chromatographed (silica gel: ethyl acetate/methanol). The pure fractions are combined and evaporated in vacuo yielding an oil, which is identified as the desired product by NMR.

Workup

  1. temperaturemaintained at ice bath temperatures
  2. temperatureThe reaction mixture is refluxed for 15 hours
  3. temperaturecooled
  4. customquenched with water (0.93 ml), aqueous sodium hydroxide (15% solution, 0.93 ml) and water (2.79 ml)
  5. filtrationfiltered
  6. washThe solid is washed with ether
  7. customthe combined filtrate dried
  8. filtrationfiltered
  9. customevaporated in vacuo
  10. customchromatographed (silica gel: ethyl acetate/methanol)
  11. customevaporated in vacuo
  12. customyielding an oil, which

Sources & evidence

ORD record
ord-b223567be6d64e149a771d6a910d490e
Source dataset
uspto-grants-1988_11
Patent number
US04788187

Reaction notes

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