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Hydrochloric Acid → HCID 57497648, 화합물

HRID 743338
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HRID 743338 반응식
[CH3:1][N:2]([CH2:4][CH:5]([OH:25])[CH2:6][O:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:3].[ClH:26]>C(OCC)(=O)C.O1CCOCC1>[ClH:26].[CH3:1][N:2]([CH2:4][CH:5]([OH:25])[CH2:6][O:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 10667347HCID 10667347, 화합물

생성물 1

HCID 57497648HCID 57497648, 화합물수율 94%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매

실험 절차

0.225 g of 3-(N,N-dimethylamino)-1-[2-(5-phenylpentyl)phenoxy]-2-propanol [prepared as described in step (b) above] was dissolved in a small amount of ethyl acetate, and 0.25 ml of a 4N solution of hydrogen chloride in dioxane was added to the solution. The mixture was then concentrated by distillation under reduced pressure. Pentane was added to the resulting concentrate, and the mixture was shaken and then the upper pentane layer was removed. The operation was repeated twice and the resulting oil was dried in vacuo, to give 0.235 g (yield 94%) of the title compound as a colorless oil.

후처리

  1. additionwas added to the solution
  2. concentrationThe mixture was then concentrated by distillation under reduced pressure
  3. additionPentane was added to the resulting
  4. concentrationconcentrate
  5. customthe upper pentane layer was removed
  6. customthe resulting oil was dried in vacuo

출처 및 근거

ORD 기록
ord-6a0f77d5a8fa4d5f9d027d78187be3a2
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556864

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