Triphenylphosphine → 2-(3-Nitrophenyl)ethan-1-amine

HRID 369727노트

반응식

HRID 369727 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][CH:14]=1)[CH2:7][CH2:8][N:9]=[N+]=[N-])([O-:3])=[O:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[N+:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][CH:14]=1)[CH2:7][CH2:8][NH2:9])([O-:3])=[O:2]

참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 224575343-Nitrophenethyl azide

생성물 1

HCID 129500662-(3-Nitrophenyl)ethan-1-amine수율 80.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 3-nitrophenethyl azide (0.9 g, 4.69 mmol), triphenyl phosphine (1.22 g, 4.66 mmol) and CH2Cl2 (80 mL) was stirred at room temperature for 3 days. Solvent was removed and the residue was taken up in EtOH (20 mL). The solution was heated to 70° C., added 2M NaOH aqueous solution (10 mL) and stirred at room temperature for 2 hrs. A 10% HCl aqueous solution (20 mL) was then added and refluxed for 2 hrs. After the mixture cool to room temperature, it was washed with benzene, basified with 5N NaOH to pH-12, extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to give the product (0.63 g) as a yellow oil.

후처리

  1. customSolvent was removed
  2. temperatureThe solution was heated to 70° C.
  3. additionadded 2M NaOH aqueous solution (10 mL)
  4. stirringstirred at room temperature for 2 hrs
  5. additionA 10% HCl aqueous solution (20 mL) was then added
  6. temperaturerefluxed for 2 hrs
  7. temperatureAfter the mixture cool to room temperature
  8. washit was washed with benzene
  9. extractionextracted with ethyl acetate
  10. dry with materialThe organic layer was dried over Na2SO4
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e4762eb872244a0d8ddfd5713acab851
출처 데이터셋
uspto-grants-2000_10
특허 번호
US06140318

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