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2,3-Difluoro-6-methoxyphenylacetic acid → 2-(2,3-Difluoro-6-methoxyphenyl)ethanol

HRID 921175
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HRID 921175 반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([O:9][CH3:10])[C:3]=1[CH2:11][C:12](O)=[O:13].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([O:9][CH3:10])[C:3]=1[CH2:11][CH2:12][OH:13]
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참가 물질

4

반응물 2

HCID 38035492,3-Difluoro-6-methoxyphenylacetic acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 1172810202-(2,3-Difluoro-6-methoxyphenyl)ethanol수율 87%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
60 °C

실험 절차

To a solution of 2-(2,3-difluoro-6-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-(2,3-difluoro-6-methoxyphenyl)ethanol (810 mg, 4.30 mmol, 87% yield) as a clear viscous oil. Used as is in the next step without further purification. 1H NMR (500 MHz, CDCl3) δ 7.01 (q, J=9.2 Hz, 1H), 6.62-6.53 (m, 1H), 3.92-3.75 (m, 5H), 3.00 (td, J=6.6, 1.9 Hz, 2H), 1.65 (t, J=5.7 Hz, 1H).

후처리

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

출처 및 근거

ORD 기록
ord-4bb99150f12f44d09de953b43635a720
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273067B2

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