Water → HCID 12331750, compound

HRID 441634Notes

Reaction equation

HRID 441634 reaction equation
O.[OH-].[Na+].[OH:4][C:5]1[CH:18]=[CH:17][C:8]2[O:9][C:10]3[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][C:11]=3[C:7]=2[CH:6]=1.[ClH:19].[N:20]1([CH2:26][CH2:27][CH2:28][Cl:29])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1>C1(C)C=CC=CC=1>[ClH:29].[ClH:19].[N:20]1([CH2:26][CH2:27][CH2:28][O:16][C:13]2[CH:14]=[CH:15][C:10]3[O:9][C:8]4[CH:17]=[CH:18][C:5]([O:4][CH2:28][CH2:27][CH2:26][N:20]5[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]5)=[CH:6][C:7]=4[C:11]=3[CH:12]=2)[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1

Participants

6

Procedure

To 200 ml of water containing 13.0 g (0.33 mole) of sodium hydroxide and 12.0 g (0.06 mole) of 2,8-dihydroxydibenzofuran are added 250 ml of toluene and 29.7 g (0.15 mole) of 3-piperidinopropyl chloride hydrochloride, and the heterogeneous reaction mixture is heated to reflux with stirring for 24 hours. When cool, the organic layer is washed with water, dried over magnesium sulfate then concentrated in vacuo. The remaining oily residue is dissolved in ether and treated with ethereal HCl to give the desired product which is recrystallized twice from methanol-ethyl acetate yielding 2,8-bis(3-piperidinopropoxy(dibenzofuran dihydrochloride, M.P. 245°-246.5° C.

Workup

  1. temperaturethe heterogeneous reaction mixture is heated
  2. temperatureto reflux
  3. temperatureWhen cool
  4. washthe organic layer is washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationthen concentrated in vacuo
  7. dissolutionThe remaining oily residue is dissolved in ether
  8. additiontreated with ethereal HCl

Sources & evidence

ORD record
ord-01cb371dff2a427cb0b5e52b2106f7b4
Source dataset
uspto-grants-1977_08
Patent number
US04041165

Reaction notes

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