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3-Fluorosalicylaldehyde → 2-Fluoro-6-(1-hydroxyethyl)phenol

HRID 1453091
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HRID 1453091 반응식
[CH3:1][Li].[F:3][C:4]1[CH:11]=[CH:10][CH:9]=[C:6]([CH:7]=[O:8])[C:5]=1[OH:12]>C1COCC1>[F:3][C:4]1[CH:11]=[CH:10][CH:9]=[C:6]([CH:7]([OH:8])[CH3:1])[C:5]=1[OH:12]
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참가 물질

4

반응물 2

HCID 5877883-FluorosalicylaldehydeHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 450831602-Fluoro-6-(1-hydroxyethyl)phenol수율 99%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Methyl lithium (25.5 mL, 35.7 mmol, 1.4M in ether) was added to a cooled −78° C. solution of 3-fluorosalicylaldehyde (2 g, 14.3 mmol) dissolved in THF (50 mL). The reaction mixture was stirred for 3 hours and then warmed up to room temperature. After 3 hours the reaction was quenched with saturated NH4Cl and extracted with EtOAc. The organic extracts were washed with 1N HCl, brine, dried over Na2SO4 and concentrated to an oil. The oil was purified by flash column chromatography (0% to 20% EtOAc in hexanes) to give the title compound as a clear oil (2.2 g, 99%). 1H NMR (400 MHz, CDCl3): δ 1.58 (d, J=6.6 Hz, 3H), 2.68 (s, 1H), 5.13 (m, 1H), 6.78 (td, J=7.8, 4.8 Hz, 1H), 6.87 (d, J=7.6, 1H), 6.99 (m, 1H), 7.33 (s, 1H).

후처리

  1. customAfter 3 hours the reaction was quenched with saturated NH4Cl
  2. extractionextracted with EtOAc
  3. washThe organic extracts were washed with 1N HCl, brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated to an oil
  6. customThe oil was purified by flash column chromatography (0% to 20% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-694ffaa9e1e84007b910080fc9491dc5
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07473790B2

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