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Hydrochloric Acid → 4'-Chloro-3-ethylbiphen-4-ylamine

HRID 72289
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HRID 72289 반응식
[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]2[CH:11]=[C:10]([CH2:12][CH3:13])[C:9]([NH:14]C(=O)C)=[CH:8][CH:7]=2)=[CH:4][CH:3]=1.Cl>O1CCOCC1>[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]2[CH:11]=[C:10]([CH2:12][CH3:13])[C:9]([NH2:14])=[CH:8][CH:7]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 59450487N-(4'-chloro-3-ethylbiphen-4-yl)acetamide

생성물 1

HCID 594504954'-Chloro-3-ethylbiphen-4-ylamine수율 97.1%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To a solution of N-(4′-chloro-3-ethylbiphen-4-yl)acetamide (18 g, 0.06 mol) in dioxane (126 ml), is added concentrated hydrochloric acid (36 ml) and the reaction mixture is heated at reflux for 2 hours. The dioxane is evaporated under reduced pressure. The residue is diluted with water, the solution made basic by addition of 2N aqueous potassium hydroxide solution and extracted with ethyl acetate (3×500 ml). The organic extracts are combined and concentrated under reduced pressure to give 4′-chloro-3-ethylbiphen-4-ylamine (13.5 g).

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후처리

  1. temperaturethe reaction mixture is heated
  2. temperatureat reflux for 2 hours
  3. customThe dioxane is evaporated under reduced pressure
  4. additionThe residue is diluted with water
  5. additionthe solution made basic by addition of 2N aqueous potassium hydroxide solution
  6. extractionextracted with ethyl acetate (3×500 ml)
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-174230f29d8d42999a762870b73e9c18
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828908B2

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