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Ethanol → HCID 57562941, 화합물

HRID 1962224
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HRID 1962224 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-fcc077205d0446f4bb9a4d1f0f8a0e07
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415365B2

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