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3-Bromo-4-chlorobenzamide → 3-Bromo-4-chlorobenzylamine

HRID 564499
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HRID 564499 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[Cl:11])[C:5]([NH2:7])=O>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][NH2:7])[CH:8]=[CH:9][C:10]=1[Cl:11]
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참가 물질

3

반응물 1

HCID 532166633-Bromo-4-chlorobenzamide

생성물 1

HCID 578133923-Bromo-4-chlorobenzylamine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

To 3-bromo-4-chlorobenzamide (1.6 g, 6.8 mmol) in THF (10 mL) was added borane dimethyl sulfide complex (1.36 mL, 13.6 mmol) at room temperature. The mixture was then heated to 60° C. for 8 days. The solvent was pumped off and the reaction cautiously quenched with ethanol. When bubbling ceased, 1N HCl was added until pH was ˜2. The mixture was stirred at 50° C. for 4 h. The mixture was partitioned between EtOAc and water. The aqueous phase was washed 3× with EtoAC. The aqueous was then adjusted to pH 10 with 2N NaOH and extracted 3× with EtOAc. The combined organics phases were washed with brine (1×) and dried over anhydrous Na2SO4, filtered, and concentrated to afford the title compound as a clear oil. LC-MS m/z 219.6 (M+H)+, 1.41 min (ret time).

후처리

  1. customthe reaction
  2. customcautiously quenched with ethanol
  3. customWhen bubbling
  4. addition1N HCl was added until pH was ˜2
  5. customThe mixture was partitioned between EtOAc and water
  6. washThe aqueous phase was washed 3× with EtoAC
  7. extractionextracted 3× with EtOAc
  8. washThe combined organics phases were washed with brine (1×)
  9. dry with materialdried over anhydrous Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ed78bd4603144d18a6f6e3ceea211d2d
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08067408B2

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