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Tetrabutylammonium Fluoride → HCID 69221542, 화합물

HRID 132853
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HRID 132853 반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][C:11]1[C:12]([O:30][CH3:31])=[N:13][C:14]([C:26]([F:29])([F:28])[F:27])=[CH:15][C:16]=1[CH2:17][O:18][Si](C(C)(C)C)(C)C)=[O:7])([CH3:4])([CH3:3])[CH3:2].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][C:11]1[C:12]([O:30][CH3:31])=[N:13][C:14]([C:26]([F:27])([F:28])[F:29])=[CH:15][C:16]=1[CH2:17][OH:18])=[O:7])([CH3:3])([CH3:4])[CH3:2]
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참가 물질

4

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 69224268HCID 69224268, 화합물

생성물 1

HCID 69221542HCID 69221542, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of the compound from Step K above (1.12 g, 2.41 mmol) in tetrahydrofuran (20 mL) was added tetrabutylammonium fluoride (11.0M in tetrahydrofuran, 2.41 mL, 2.41 mmol). The reaction was then stirred at room temperature for 10 min and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel; 20% to 40% ethyl acetate/hexanes gradient elution) to afford the title compound. 1H NMR (400 MHz, CDCl3) δ 7.38 (s, 1H), 4.87 (br s, 1H), 4.76 (d, 2H, J=6 Hz), 4.02 (s, 3H), 3.54 (t, 1H), 3.35 (m, 2H), 2.88 (t, 2H, J=6 Hz), 1.38 (s, 9H).

후처리

  1. concentrationconcentrated under reduced pressure
  2. customThe residue was purified by flash chromatography (silica gel; 20% to 40% ethyl acetate/hexanes gradient elution)

출처 및 근거

ORD 기록
ord-58482d8711b649ef85974358671decc7
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07388019B2

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