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Water → 3-(Methanesulfonyl)-4-methylaniline

HRID 1814658
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HRID 1814658 반응식
[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([N+:11]([O-])=O)[CH:8]=[CH:7][C:6]=1[CH3:14])(=[O:4])=[O:3].O.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C>C(O)C>[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([CH:8]=[CH:7][C:6]=1[CH3:14])[NH2:11])(=[O:3])=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 10340Sodium CarbonateHCID 14026543HCID 14026543, 화합물

생성물 1

HCID 222603163-(Methanesulfonyl)-4-methylaniline수율 84.5%

시약·촉매·용매 1

HCID 702Ethanol용매

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
75 °C

실험 절차

2-Methylsulfonyl-1-methyl-4-nitrobenzene (500 mg, 2.3 mmol) was dissolved in absolute ethanol (15 mL). Stannous chloride (2.6 g, 11.6 mmol) was added and the reaction mixture was stirred at 75° C. for 4 hours. The mixture was poured into water (50 mL), pH was adjusted with a saturated solution of sodium carbonate to basic reaction, followed by addition of ethyl acetate (150 mL). The organic phase was extracted with water (2×50 mL), dried (MgSO4) and concentrated in vacuo to give 0.36 g of 3-methylsulfonyl-4-methylaniline as an oil.

후처리

  1. extractionThe organic phase was extracted with water (2×50 mL)
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-da816327c9f240aca9796cde8357ff41
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06875760B2

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