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6-Fluoro-benzofuran-3-one oxime → 6-Fluoro-2,3-dihydrobenzofuran-3-amine

HRID 1928884
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HRID 1928884 반응식
[F:1][C:2]1[CH:12]=[CH:11][C:5]2[C:6](=[N:9]O)[CH2:7][O:8][C:4]=2[CH:3]=1.[H][H]>O1CCCC1.CO.[Ni]>[F:1][C:2]1[CH:12]=[CH:11][C:5]2[CH:6]([NH2:9])[CH2:7][O:8][C:4]=2[CH:3]=1
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참가 물질

6

반응물 2

HCID 866341876-Fluoro-benzofuran-3-one oximeHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 552634306-Fluoro-2,3-dihydrobenzofuran-3-amine수율 33.7%

시약·촉매·용매 3

HCID 935Nickel촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of the above described 6-fluoro-benzofuran-3-one oxime (5.38 g, 32 mmol; HPLC 1.489 min) and Raney-Nickel (2.4 g) in tetrahydrofuran (125 mL) and methanol (125 mL) was hydrogenated at 100 bar hydrogen-pressure at 50° C. for 18 h. Filtered the catalyst off, washed with methanol and tetrahydrofuran, all volatiles very removed in vacuum to give the crude product which was purified by Si—NH2 column chromatography with n-heptane/ethyl acetate to give the title compound as a light brown liquid (1.65 g, 34%, HPLC 0.367 min 100%), MS (ISP) m/e=154.0 [(M+H)+].

후처리

  1. additionA mixture of the
  2. filtrationFiltered the catalyst off,
  3. washwashed with methanol and tetrahydrofuran
  4. customall volatiles very removed in vacuum
  5. customto give the crude product which
  6. customwas purified by Si—NH2 column chromatography with n-heptane/ethyl acetate

출처 및 근거

ORD 기록
ord-f4a12df88196476ab68f0114dd12cf4e
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08183380B2

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