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4,5-Difluoro-2-methoxyphenylacetic acid → 2-(4,5-Difluoro-2-methoxyphenyl)ethan-1-ol

HRID 921182
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HRID 921182 반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([CH2:9][C:10](O)=[O:11])=[C:4]([O:13][CH3:14])[CH:3]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([CH2:9][CH2:10][OH:11])=[C:4]([O:13][CH3:14])[CH:3]=1
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참가 물질

4

반응물 2

HCID 177507674,5-Difluoro-2-methoxyphenylacetic acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 552676712-(4,5-Difluoro-2-methoxyphenyl)ethan-1-ol수율 86%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
60 °C

실험 절차

To a solution of 2-(4,5-difluoro-2-methoxyphenyl)acetic acid (1 g, 4.95 mmol) in THF (20 mL) at 0° C. was added 1M LAH (9.89 mL, 9.89 mmol) in THF and the resulting mixture was heated at 60° C. for 3 h. Mixture was then cooled and quenched with dropwise addition of water (0.5 mL), 1N NaOH (0.5 mL), and then 1 mL H2O. After stirring for 15 min. the mixture was filtered through celite. The filtrate was concentrated in vacuo. The residue was dried under high vacuum to afford 2-(4,5-difluoro-2-methoxyphenyl)ethanol (800 mg, 4.25 mmol, 86% yield) as a clear viscous oil. Used as is in the next step without further purification. 1H NMR (500 MHz, CDCl3) δ 7.02 (t, J=9.8 Hz, 1H), 6.71 (dd, J=12.1, 6.7 Hz, 1H), 3.87-3.82 (m, 2H), 3.81 (s, 3H), 2.85 (t, J=6.5 Hz, 2H), 1.56 (br. s., 1H).

후처리

  1. temperatureMixture was then cooled
  2. customquenched with dropwise addition of water (0.5 mL), 1N NaOH (0.5 mL)
  3. filtrationwas filtered through celite
  4. concentrationThe filtrate was concentrated in vacuo
  5. customThe residue was dried under high vacuum

출처 및 근거

ORD 기록
ord-fcff42c4b03e4b57b5e907805e54eff9
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273067B2

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