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Hydrochloric Acid → N,N-Dimethyl-3-[2-(4-phenylbutyl)phenoxy]propylamine hydrochloride

HRID 743173
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HRID 743173 반응식
[ClH:1].[CH3:2][N:3]([CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15][CH2:16][CH2:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:4]>O1CCOCC1.C(OCC)(=O)C>[ClH:1].[CH3:2][N:3]([CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15][CH2:16][CH2:17][CH2:18][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)[CH3:4]
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 9904842N,N-Dimethyl-3-[2-(4-phenylbutyl)phenoxy]propylamine

생성물 1

HCID 57497605N,N-Dimethyl-3-[2-(4-phenylbutyl)phenoxy]propylamine hydrochloride수율 89%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매

실험 절차

0.18 ml of a 4N solution of hydrogen chloride in dioxane was added to a solution of 210 mg of N,N-dimethyl-3-[2-(4-phenylbutyl)phenoxy]propylamine [prepared as described in step (a) above] in 5 ml of ethyl acetate, and the resulting mixture was concentrated by distillation under reduced pressure. The resulting residue was dissolved in a small amount of ethyl acetate, and the resulting solution was allowed to stand at room temperature. The crystals which precipitated were collected by filtration to give 210 mg (yield 89%) of the title compound as colorless crystals, melting at 104°-106° C.

후처리

  1. concentrationthe resulting mixture was concentrated by distillation under reduced pressure
  2. dissolutionThe resulting residue was dissolved in a small amount of ethyl acetate
  3. customto stand at room temperature
  4. customThe crystals which precipitated
  5. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-51271a1d059e42d39840e22a60e88f4a
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556864

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