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Lithium Hydroxide → 5-(2,5-Dichlorophenyl)pentanoic acid

HRID 1532548
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HRID 1532548 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15]C)=[O:14].[Li+].[OH-]>C1COCC1.CO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14]
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참가 물질

5

반응물 2

HCID 3939Lithium HydroxideHCID 22013526Methyl 5-(2,5-Dichlorophenyl)pentanoate

생성물 1

HCID 220135385-(2,5-Dichlorophenyl)pentanoic acid수율 70%

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 5-(2,5-Dichlorophenyl)pentanoate (1.10 g, 4.2 mmol) was dissolved in 20 ml THF and 7 mL methanol. 1 N LiOH (12 mL) was added dropwise and the reaction was stirred at room temperature for 2 days. The reaction was worked-up by acidification with 2 N HCl and removal of most of the THF and methanol on a rotary evaporator followed by extraction of the aqueous residue with ethyl acetate. The organic phase was washed with water and saturated brine, dried over sodium sulfate and concentrated to a residue. Flash chromatography (silica gel; hexane/toluene (19/1) with 1% acetic acid) of the residue gave 725 mg (70%) of a white solid.

후처리

  1. customThe reaction was worked-up by acidification with 2 N HCl and removal of most of the THF and methanol
  2. customon a rotary evaporator
  3. extractionfollowed by extraction of the aqueous residue with ethyl acetate
  4. washThe organic phase was washed with water and saturated brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated to a residue

출처 및 근거

ORD 기록
ord-dbca058e47504eefbffa576f46740a05
출처 데이터셋
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06204005B1

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