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Hydrogen Bromide → 4'-Bromo-2'-phenylacetanilide

HRID 1518630
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반응식

HRID 1518630 반응식
[C:1]1([C:7]2[CH:16]=[CH:15][CH:14]=[CH:13][C:8]=2[NH:9][C:10](=[O:12])[CH3:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BrH:17]>C(O)(=O)C.C(Cl)(Cl)(Cl)Cl>[C:1]1([C:7]2[CH:16]=[C:15]([Br:17])[CH:14]=[CH:13][C:8]=2[NH:9][C:10](=[O:12])[CH3:11])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 260Hydrogen BromideHCID 164472-Acetamidobiphenyl

생성물 1

HCID 2424004'-Bromo-2'-phenylacetanilide수율 91.3%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 5943Carbon Tetrachloride용매

실험 절차

2-Phenyl-N-acetylaniline (6.21 g, 29.40 mmol) was dissolved in acetic acid (70 mL). Thereto was dropwise added under ice bath a separately prepared solution of hydrogen bromide (6.14 g, 38.42 mmol) dissolved in carbon tetrachloride (19.21 mL) and the mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure, to the residue was added water (20 mL) and subsequently ethanol (30 mL), and the mixture was stirred under ice bath for 1 hour. The precipitate was collected by filtration, washed with ethanol/water (=1:1), dried under reduced pressure to obtain 2-phenyl-4-bromo-N-acetylaniline (7.79 g).

후처리

  1. concentrationThe solution was concentrated under reduced pressure, to the residue
  2. additionwas added water (20 mL) and subsequently ethanol (30 mL)
  3. stirringthe mixture was stirred under ice bath for 1 hour
  4. filtrationThe precipitate was collected by filtration
  5. washwashed with ethanol/water (=1:1)
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-c1a270181535486187596470ab6be54a
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09072734B2

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