Tetrahydrofuran → 4,5-Dichloro-2-methylaniline

HRID 245959

반응식

HRID 245959 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[C:5]([CH3:11])=[CH:4][C:3]=1[Cl:12].C1COCC1.[NH4+].[Cl-]>CO.O.[Fe]>[Cl:12][C:3]1[C:2]([Cl:1])=[CH:7][C:6]([NH2:8])=[C:5]([CH3:11])[CH:4]=1

참가 물질

7

반응 조건

온도
100 °C

실험 절차

To a partial suspension of 1,2-dichloro-4-methyl-5-nitrobenzene (2.0 g, 9.71 mmol) in MeOH (25 ml), water (25 ml), and THF (10 ml) was added NH4Cl (5.19 g, 97.1 mmol) followed by iron powder (2.71 g, 48.5 mmol). The heterogeneous reaction mixture was heated at 100° C. for 3 h then cooled to room temperature and filtered over a Buchner funnel, rinsing with MeOH. The filtrate was diluted with water and saturated aqueous NaHCO3 then extracted with CH2Cl2 (3×). The combined organics were dried over MgSO4 and concentrated to afford 1.69 g (99%) of 4,5-dichloro-2-methylaniline as a white solid. 1H NMR (CDCl3, 300 MHz): δ (ppm) 7.10 (s, 1H), 6.75 (s, 1H), 3.74 (br. s., 2H), 2.12 (s, 3H).

후처리

  1. temperaturethen cooled to room temperature
  2. filtrationfiltered over a Buchner funnel
  3. washrinsing with MeOH
  4. additionThe filtrate was diluted with water and saturated aqueous NaHCO3
  5. extractionthen extracted with CH2Cl2 (3×)
  6. dry with materialThe combined organics were dried over MgSO4
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ee13f308c706464ab23b5a7a4732734e
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08658646B2

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