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Hexane → 5-Fluoro-3-hydroxy-6-methoxy-quinoline-4-carbaldehyde

HRID 1422914
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HRID 1422914 반응식
[F:1][C:2]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4]([CH2:15][OH:16])=[C:5]([OH:14])[CH:6]=[N:7]2.C(OCC)(=O)C.CCCCCC>CC(C)=O.[O-2].[O-2].[Mn+4]>[F:1][C:2]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4]([CH:15]=[O:16])=[C:5]([OH:14])[CH:6]=[N:7]2
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참가 물질

6

반응물 3

HCID 8058HexaneHCID 8857Ethyl AcetateHCID 672487085-Fluoro-4-hydroxymethyl-6-methoxy-quinolin-3-ol

생성물 1

HCID 866715305-Fluoro-3-hydroxy-6-methoxy-quinoline-4-carbaldehyde수율 42.1%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 180
Acetone
용매

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온도
35 °C

실험 절차

Manganese dioxide (299 mg, 4.3 mmol, 10.0 eq) is added at room temperature to a stirred solution of 5-fluoro-4-hydroxymethyl-6-methoxy-quinolin-3-ol (120 mg, 0.43 mmol, 1.0 eq) in acetone (12 mL) and the resulting mixture is stirred at 35° C. for 17 hours. The solid is filtered off, washed with acetone (3×10 mL) and the filtrate is concentrated to give a residue that is purified by column chromatography (silica gel, eluent: ethyl acetate:hexane, 1:3, v/v) to afford 5-fluoro-3-hydroxy-6-methoxy-quinoline-4-carbaldehyde as a yellow solid (40 mg, 42% yield).

후처리

  1. filtrationThe solid is filtered off
  2. washwashed with acetone (3×10 mL)
  3. concentrationthe filtrate is concentrated
  4. customto give a residue that
  5. customis purified by column chromatography (silica gel, eluent

출처 및 근거

ORD 기록
ord-962e0edbf0474130850465bef18c5f25
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927541B2

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