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

HRID 27061노트

반응식

HRID 27061 반응식
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]

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 205450052-(4-Bromobutoxy)-2'-chlorobibenzyl

생성물 1

HCID 30553461-Butanamine, 4-(2-(2-(2-chlorophenyl)ethyl)phenoxy)-N,N-dimethyl-, hydrochloride수율 93%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-ac795e5570e145a788b92da318c90f4b
출처 데이터셋
uspto-grants-1980_09
특허 번호
US04220603

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