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Sodium Hydroxide → 2-Amino-4-bromo-6-fluorophenol

HRID 323082
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HRID 323082 반응식
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[C:5]([OH:11])=[C:4]([F:12])[CH:3]=1.[Sn](Cl)Cl.[OH-].[Na+]>C(O)C>[NH2:8][C:6]1[CH:7]=[C:2]([Br:1])[CH:3]=[C:4]([F:12])[C:5]=1[OH:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24479Stannous ChlorideHCID 6881164-Bromo-2-fluoro-6-nitrophenol

생성물 1

HCID 27376372-Amino-4-bromo-6-fluorophenol수율 82.1%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

A mixture of 4-bromo-2-fluoro 6-nitrophenol(1 g, 4.2 mmol) and tin (II) chloride (4.78 g, 21.2 mmol) in ethanol(50 mL) was heated at 80° C. under argon. After 2 hours, the starting material had disappeared and the solution was allowed to cool down and then poured into ice. The pH was made slightly basic (pH7-8), by addition of solid NaOH, before being extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4 and filtered. The solvent was evaporated and chromatography of the resulting solid on silica gel (4% MeOH/CH2Cl2) gave the desired product(710 mg, 82%). 1H NMR (CD3OD): d 6.51-6.40 (m, 2H).

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후처리

  1. temperatureto cool down
  2. additionpoured into ice
  3. extractionbefore being extracted with ethyl acetate
  4. washThe organic phase was washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-c61d5d4db10c467bbcef238e2c9e6510
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06211373B1

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