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Hydrochloric Acid → 1-(3-Chlorophenyl)butan-1-amine

HRID 659977
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HRID 659977 반응식
F[C:2]1[CH:3]=[C:4]([C:8](=O)[CH2:9][CH2:10][CH3:11])[CH:5]=[CH:6][CH:7]=1.C([O-])(=O)C.[NH4+:17].C([BH3-])#N.[Na+].[ClH:22]>CO>[Cl:22][C:2]1[CH:3]=[C:4]([CH:8]([NH2:17])[CH2:9][CH2:10][CH3:11])[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 517165Ammonium AcetateHCID 5003444Sodium cyanoborohydrideHCID 204362041-(3-Fluorophenyl)butan-1-one

생성물 1

HCID 588532391-(3-Chlorophenyl)butan-1-amine수율 28%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 1-(3-fluorophenyl)butan-1-one (430 mg, 2.4 mmol) and ammonium acetate (1.09 g, 14.1 mmol) in methanol (10 mL) under nitrogen was added sodium cyanoborohydride (2.35 ml, 1M solution in THF, 2.35 mmol). The solution was stirred at room temperature for 38 h. after which time conc. HCl was added to give a pH˜2. After bubbling had ceased the solvent was removed under reduced pressure and the residue dissolved in ethyl acetate and water. The organic phase was collected and the aqueous phase washed with ethyl acetate (20 mL). The aqueous phase was basified to pH˜10 with solid KOH and the product extracted into ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried (Na2SO4) and concentrated to give a pure product (120 mg, 28%).

후처리

  1. additionwas added
  2. customto give a pH˜2
  3. customAfter bubbling
  4. customwas removed under reduced pressure
  5. dissolutionthe residue dissolved in ethyl acetate
  6. customThe organic phase was collected
  7. washthe aqueous phase washed with ethyl acetate (20 mL)
  8. extractionthe product extracted into ethyl acetate (3×20 mL)
  9. washwashed with brine
  10. dry with materialdried (Na2SO4)
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-526cc426781647b0b7e89589d9dc8680
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084456B2

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