HCID 22735649, 화합물 → 5-Bromo-2-[(3-chloropropyl)sulfanyl]aniline

HRID 50971노트

반응식

HRID 50971 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH2:10][CH2:11][Cl:12])=[C:4]([N+:13]([O-])=O)[CH:3]=1>CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH2:10][CH2:11][Cl:12])=[C:4]([CH:3]=1)[NH2:13]

참가 물질

3

실험 절차

4-Bromo-1-[(3-chloropropyl)sulfanyl]-2-nitrobenzene (1.97 g, 7.1 mmol) was dissolved in MeOH (25 mL). The reaction flask was evacuated with nitrogen, and Pd(OH)2 on carbon (400 mg) was added. The reaction flask was evacuated with nitrogen several time before being subjected to an atmosphere of H2 (50 psi). The flask was shaken on a parr apparatus for 72 hrs. The reaction was filtered over a bed of celite and the residue was washed with MeOH (5 mL). The supernant was concentrated, and the crude, balck residue was purified by column chromatography (50-20% hexanes-CH2Cl2), to afford 5-bromo-2-[(3-chloropropyl)sulfanyl]aniline (1.28 g, 73%) as a clear oil. 1H NMR (CDCl3, 300 Mhz) δ7.20 (d, 1H, 8.0 Hz), 6.88 (d, 1H, 2.0 Hz), 6.79 (dd, 1H, 2.0 Hz, 8.0 Hz), 4.41 (s, 2H), 3.64 (t, 2H, 6.6 Hz), 2.86 (t, 2H, 7.0 Hz), 1.94-1.99 (m, 2H) ppm.

후처리

  1. customThe reaction flask was evacuated with nitrogen, and Pd(OH)2 on carbon (400 mg)
  2. additionwas added
  3. customThe reaction flask was evacuated with nitrogen several time
  4. filtrationThe reaction was filtered over a bed of celite
  5. washthe residue was washed with MeOH (5 mL)
  6. concentrationThe supernant was concentrated
  7. customthe crude, balck residue was purified by column chromatography (50-20% hexanes-CH2Cl2)

출처 및 근거

ORD 기록
ord-9de867f0fe5a4143af43a955f851091f
출처 데이터셋
uspto-grants-2004_03
특허 번호
US06713471B1

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