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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-Isopropyl-4-nitroaniline

HRID 1910756
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HRID 1910756 반응식
[CH:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:5]=1[NH:13]C(=O)C)([CH3:3])[CH3:2].Cl>C(O)C>[CH:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:5]=1[NH2:13])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 45074589N-(2-Isopropyl-4-nitrophenyl)acetamide

생성물 1

HCID 223794772-Isopropyl-4-nitroaniline수율 86.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

N-(2-Isopropyl-4-nitro-phenyl)-acetamide (3 g, 13.5 mmol) was dissolved in absolute ethanol (20 mL) and 5N hydrochloric acid (20 mL) was added. The mixture was heated to reflux overnight, cooled to r.t. then concentrated in vacuo to remove the ethanol. The mixture was basified with dilute sodium hydroxide solution and extracted with ethyl acetate. The combined organic layers were washed with water and brine solution, dried over sodium sulfate and concentrated. The crude product was purified by column chromatography on silica gel (60-120 mesh), eluting with 17% ethyl acetate/petroleum ether to afford 2-isopropyl-4-nitro-phenylamine (2.1 g, 85%).

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux overnight
  3. concentrationthen concentrated in vacuo
  4. customto remove the ethanol
  5. extractionextracted with ethyl acetate
  6. washThe combined organic layers were washed with water and brine solution
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated
  9. customThe crude product was purified by column chromatography on silica gel (60-120 mesh)
  10. washeluting with 17% ethyl acetate/petroleum ether

출처 및 근거

ORD 기록
ord-835bfd5b52ea4dccb6f622c06d40901d
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604029B2

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