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Ethanol → HCID 57562941, 화합물

HRID 1770819
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HRID 1770819 반응식
[NH2:1][S:2]([C:5]1[CH:6]=[C:7]([N+:13]([O-])=O)[CH:8]=[C:9]([CH3:12])[C:10]=1[F:11])(=[O:4])=[O:3].C(O)C.[Cl-].[NH4+]>[Fe].O>[NH2:1][S:2]([C:5]1[CH:6]=[C:7]([CH:8]=[C:9]([CH3:12])[C:10]=1[F:11])[NH2:13])(=[O:4])=[O:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 57562895HCID 57562895, 화합물

생성물 1

HCID 57562941HCID 57562941, 화합물

시약·촉매·용매 2

HCID 23925Iron촉매HCID 962Water용매

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온도
60 °C

실험 절차

To a heterogeneous solution of 3-aminosulfonyl-4-fluoro-5-methylnitrobenzene (27) (0.5 g, 2 mmol) in of ethanol:water (50 mL, each) were added iron powder (1.08 g, 20 mmol), and ammonium chloride (1.08 g, 20 mmol) at room temperature. The resulting heterogeneous mixture was then stirred at 60° C. for 2 hours, filtered through celite (when hot), washed with ethanol (2×50 mL) and then the solvent was removed under reduced pressure. The residue upon dilution with water was extracted with ethyl acetate (3×50 mL), and the organic phase was dried over anhydrous sodium sulfate and concentrated under a reduced pressure to obtain 3-aminosulfonyl-4-fluoro-5-methylaniline (28). LCMS: purity: 85%; MS (m/z): 205 (MH+).

후처리

  1. filtrationfiltered through celite (when hot)
  2. washwashed with ethanol (2×50 mL)
  3. customthe solvent was removed under reduced pressure
  4. extractionThe residue upon dilution with water was extracted with ethyl acetate (3×50 mL)
  5. dry with materialthe organic phase was dried over anhydrous sodium sulfate
  6. concentrationconcentrated under a reduced pressure

출처 및 근거

ORD 기록
ord-5636bb7326d3455a9c43ca8a48dd1cd9
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09248190B2

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