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Methanol → 1-Methanesulfonyl-5-methoxy-phenylamine

HRID 418076
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HRID 418076 반응식
[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([N+]([O-])=O)[CH:8]=[C:7]([O:14][CH3:15])[CH:6]=1)(=[O:4])=[O:3].[Cl-].[NH4+:17].CO>[Zn].O>[CH3:1][S:2]([C:5]1([NH2:17])[CH:6]=[C:7]([O:14][CH3:15])[CH:8]=[CH:9][CH2:10]1)(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 887MethanolHCID 25517Ammonium ChlorideHCID 578630801-(Methanesulfonyl)-3-methoxy-5-nitrobenzene

생성물 1

HCID 666496371-Methanesulfonyl-5-methoxy-phenylamine수율 76%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 962Water용매2회

실험 절차

To a mixture of 1-methanesulfonyl-3-methoxy-5-nitro-benzene (1.5 g, 6.48 mmol), zinc dust (4.3 g, 64.87 mmol), and ammonium chloride (5.2 g, 97.31 mmol) were added methanol (20.32 mL) and water (9.9 mL) at room temperature. After addition of water, the reaction was exothermic. The suspension was stirred for 30 min and the reaction mixture was filtered through the Celite. The filter cake was washed with water and methanol. The filtrate was concentrated to remove methanol and the residue was extracted with ethyl acetate (2×50 mL). The combined extracts were washed with brine solution (100 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to isolate 1-methanesulfonyl-5-methoxy-phenylamine (1.0 g, 76%) as a light yellow solid: ES(+)-HRMS m/e calcd for C8H12NO3S (M+H)+ 202.0533, found 202.0532.

후처리

  1. filtrationthe reaction mixture was filtered through the Celite
  2. washThe filter cake was washed with water and methanol
  3. concentrationThe filtrate was concentrated
  4. customto remove methanol
  5. extractionthe residue was extracted with ethyl acetate (2×50 mL)
  6. washThe combined extracts were washed with brine solution (100 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e5198d1f0cc34967ab0f6e775fe13335
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08093253B2

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