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Ammonium Chloride → 3-[(Dimethylamino)methyl]-4-fluoroaniline

HRID 1430556
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HRID 1430556 반응식
[NH4+].[Cl-].[F:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-])=O)=[CH:6][C:5]=1[CH2:13][N:14]([CH3:16])[CH3:15]>CCO.[Fe]>[CH3:16][N:14]([CH2:13][C:5]1[CH:6]=[C:7]([CH:8]=[CH:9][C:4]=1[F:3])[NH2:10])[CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 25517Ammonium ChlorideHCID 58998500HCID 58998500, 화합물

생성물 1

HCID 450889853-[(Dimethylamino)methyl]-4-fluoroaniline수율 72.8%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

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온도
55 °C

실험 절차

A mix of satd. NH4Cl (5.19 mL) in EtOH (8 mL) was treated with 1-(2-fluoro-5-nitrophenyl)-N,N-dimethylmethanamine (494 mg, 2.49 mmol), followed by iron powder (1.39 g, 24.93 mmol) and heated at 55° C. overnight. The mixture was cooled to RT, the solids removed via filtration through diatomaceous earth and washed with 10% MeOH/DCM. The filtrate was concentrated to dryness, the residue treated with DCM, sonicated and the resulting solid collected via filtration, washed with THF and dried to afford 3-((dimethylamino)methyl)-4-fluoroaniline (305 mg, 72% yield). MS (ESI) m/z: 169.1 [M+H]+.

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후처리

  1. additionA mix of satd
  2. temperatureThe mixture was cooled to RT
  3. customthe solids removed via filtration through diatomaceous earth
  4. washwashed with 10% MeOH/DCM
  5. concentrationThe filtrate was concentrated to dryness
  6. additionthe residue treated with DCM
  7. customsonicated
  8. filtrationthe resulting solid collected via filtration
  9. washwashed with THF
  10. customdried

출처 및 근거

ORD 기록
ord-f7c46ed6433a48c1a1365d032fcf9606
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940756B2

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