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Ammonium Chloride → (6-Fluoro-3-iodo-2-methylphenyl)methanol

HRID 1948670
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HRID 1948670 반응식
[F:1][C:2]1[C:7]([C:8](OC)=[O:9])=[C:6]([CH3:12])[C:5]([I:13])=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+].[H][H]>C(OCC)C>[F:1][C:2]1[C:7]([CH2:8][OH:9])=[C:6]([CH3:12])[C:5]([I:13])=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 25517Ammonium Chloride2회HCID 21226445Aluminium lithium hydrideHCID 59450535Methyl 6-fluoro-3-iodo-2-methylbenzoateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 59450541(6-Fluoro-3-iodo-2-methylphenyl)methanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매
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실험 절차

To a solution of the product from Step B (5.5 g, 18.7 mmol) in diethyl ether (20 ml) was carefully added lithium aluminum hydride (0.8 g, 18.7 mmol). The mixture was stirred at room temperature for 16 h. Saturated aqueous ammonium chloride solution was added dropwise until no hydrogen gas was being generated. A few more drops of saturated aqueous ammonium chloride solution were added and the mixture was stirred at room temperature for 30 min and filtered. The filtrated was dried over magnesium sulfate and concentrated to dryness to give the title compound as a colorless oil.

후처리

  1. stirringthe mixture was stirred at room temperature for 30 min
  2. filtrationfiltered
  3. dry with materialThe filtrated was dried over magnesium sulfate
  4. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-1fd73c74585946c8ba71ff1a9c74a445
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399507B2

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