Water → HCID 131714671, compound

HRID 2232252Notes

Reaction equation

HRID 2232252 reaction equation
[N:1]([CH2:4][CH2:5][CH2:6][O:7][C:8]12[CH:22]=[CH:21][CH:20]=[CH:19][CH:9]1[CH2:10][CH:11]2[CH2:12][N:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)=[N+]=[N-].[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[Na+]>C1COCC1.CCOCC>[NH2:1][CH2:4][CH2:5][CH2:6][O:7][C:8]12[CH:22]=[CH:21][CH:20]=[CH:19][CH:9]1[CH2:10][CH:11]2[CH2:12][N:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

Participants

7

Procedure

A solution of the azido benzocyclobutenylmethyl compound (0.8 g) (step 8 above) in THF (5.2 ml) is added over a period of 30 min to a suspension of LAH (0.125 g) in anhydrous ether (16.5 ml) stirred under nitrogen. The mixture is refluxed for about 2 hours and cooled. Water (0.125 ml), aqueous NaOH (15% solution, 0.125 ml) and water (3.75 ml) are added to the cooled mixture which is filtered. The solid is washed with ether and the filtrate dried over Na2SO4. The dried filtrate is filtered, evaporated in vacuo and chromatographed (silica gel) eluting with 1:1 ethyl acetate/MeOH. The pure fractions are combined and evaporated in vacuo yielding an oil. NMR analysis identifies the oil as the desired product.

Workup

  1. temperatureThe mixture is refluxed for about 2 hours
  2. temperaturecooled
  3. filtrationis filtered
  4. washThe solid is washed with ether
  5. dry with materialthe filtrate dried over Na2SO4
  6. filtrationThe dried filtrate is filtered
  7. customevaporated in vacuo
  8. customchromatographed (silica gel)
  9. washeluting with 1:1 ethyl acetate/MeOH
  10. customevaporated in vacuo
  11. customyielding an oil

Sources & evidence

ORD record
ord-36e9dd858cb648b4a7dce6eadf37d39a
Source dataset
uspto-grants-1988_11
Patent number
US04788187

Reaction notes

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