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Acetic Acid → N-Isopropyl-3-broMoaniline

HRID 365526
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인쇄 미리보기

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HRID 365526 반응식
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH:8]=[CH:9][CH:10]=1)[NH2:7].C(O)(=O)C.[CH3:15][C:16]([CH3:18])=O.C([O-])(=O)C.[Na+]>CCCCCC.CCOCC.O.C(O)C>[Br:3][C:4]1[CH:5]=[C:6]([NH:7][CH:16]([CH3:18])[CH3:15])[CH:8]=[CH:9][CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 5

HCID 176Acetic AcidHCID 180AcetoneHCID 115623-BromoanilineHCID 517045Sodium AcetateHCID 4311764Sodium borohydride

생성물 1

HCID 23291934N-Isopropyl-3-broMoaniline

시약·촉매·용매 4

HCID 702
Ethanol
용매
HCID 962Water용매
HCID 3283Diethyl Ether용매
HCID 8058Hexane용매

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온도
0 °C

실험 절차

Sodium borohydride (16.5 g, 435 mmol) was added slowly over 2 hours to a mixture of 3-bromoaniline (10 g, 58.13 mmol), ethanol (58 mL), acetic acid (50 mL, 866.1 mmol), water (140 mL), acetone (35 mL, 482.5 mmol), and sodium acetate (15.8 g, 116.2 mmol). The solution was stirred at 0° C. for 3 hours. The reaction mixture was poured into 1:1 mixture of ether and hexane containing 2N KOH. The layers were separated and the aqueous layer was extracted with ether/hexane (1:1). The combined organic layers were washed once with water and brine, dried with MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (10% ethyl acetate in hexane, Rf=0.31) to give the title compound (23.10 g, 93% as an oil:

후처리

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with ether/hexane (1:1)
  3. washThe combined organic layers were washed once with water and brine
  4. dry with materialdried with MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel chromatography (10% ethyl acetate in hexane, Rf=0.31)

출처 및 근거

ORD 기록
ord-69262a77297e40e0ad93be9708005277
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06127382

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