Dimethylamine → 1-Butanamine, 4-(2-(2-(2-chlorophenyl)ethyl)phenoxy)-N,N-dimethyl-, hydrochloride

HRID 27061Notes

Reaction equation

HRID 27061 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[Cl:21].[CH3:22][NH:23][CH3:24]>O1CCCC1>[ClH:21].[CH3:22][N:23]([CH3:24])[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[Cl:21]

Participants

4

Procedure

A solution of 3.0 g of 2-(4-bromobutoxy)-2'-chlorobibenzyl in 15 ml of 50% aqueous dimethylamine solution and 15 ml of tetrahydrofuran was stirred at room temperature for 5 hours. The reaction mixture was concentrated and to the concentrate was added 2N-NaOH solution. The product was extracted with ether, washed well with saturated sodium chloride solution and then dried over anhydrous sodium sulfate. To the ether solution was added 20% ethanolic hydrogen chloride to yield white crystals. Recrystallization from ethanol-ether gave 2.8 g (93% yield) of 2-(4-dimethylaminobutoxy)-2'-chlorobibenzyl hydrochloride, m. p. 122°-123° C.

Workup

  1. concentrationThe reaction mixture was concentrated and to the concentrate
  2. additionwas added 2N-NaOH solution
  3. extractionThe product was extracted with ether
  4. washwashed well with saturated sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. additionTo the ether solution was added 20% ethanolic hydrogen chloride
  7. customto yield white crystals
  8. customRecrystallization from ethanol-ether

Sources & evidence

ORD record
ord-ac795e5570e145a788b92da318c90f4b
Source dataset
uspto-grants-1980_09
Patent number
US04220603

Reaction notes

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