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

HRID 341685
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HRID 341685 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 refluxed 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 refluxed for 2 hours
  2. customThe dioxane is evaporated under reduced pressure
  3. additionThe residue is diluted with water
  4. additionthe solution made basic by addition of 2N aqueous potassium hydroxide solution
  5. extractionextracted with ethyl acetate (3×500 ml)
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-833ac59a57cc467d810bd8ae02b19839
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895761B2

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