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Sodium borohydride → HCID 58687965, 화합물

HRID 132848
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HRID 132848 반응식
[Br:1][C:2]1[C:9]([O:10][CH3:11])=[N:8][C:7]([C:12]([F:15])([F:14])[F:13])=[C:6]([Br:16])[C:3]=1[CH:4]=[O:5].[BH4-].[Na+]>C(O)C>[Br:1][C:2]1[C:9]([O:10][CH3:11])=[N:8][C:7]([C:12]([F:15])([F:14])[F:13])=[C:6]([Br:16])[C:3]=1[CH2:4][OH:5]
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 534038503,5-Dibromo-2-methoxy-6-(trifluoromethyl)pyridine-4-carbaldehyde

생성물 1

HCID 58687965HCID 58687965, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 3,5-dibromo-2-methoxy-6-(trifluoromethyl)isonicotinaldehyde (980 mg, 2.7 mmol) in ethanol (10 mL) was added sodium borohydride (102 mg, 2.7 mmol). The reaction mixture was stirred for 20 min, concentrated, and the residue was purified by flash chromatography (silica gel; 50% ethyl acetate/hexanes as eluant) to yield the title compound. 1H NMR (400 MHz, CDCl3) δ 5.10 (s, 2H), 4.05 (s, 3H), 2.32 (br s, 1H).

후처리

  1. concentrationconcentrated
  2. customthe residue was purified by flash chromatography (silica gel; 50% ethyl acetate/hexanes as eluant)

출처 및 근거

ORD 기록
ord-6ccd91e590644054bdb496793e368843
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07388019B2

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