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Water → 4-[(4-Fluorophenyl)(hydroxy)methyl]benzonitrile

HRID 561497
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HRID 561497 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[CH:4][CH:3]=1.C([Li])CCC.[C:14]([C:16]1[CH:23]=[CH:22][C:19]([CH:20]=[O:21])=[CH:18][CH:17]=1)#[N:15].O>O1CCCC1.CCCCCC.C(OCC)(=O)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:20]([OH:21])[C:19]2[CH:22]=[CH:23][C:16]([C:14]#[N:15])=[CH:17][CH:18]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 962WaterHCID 99931-Bromo-4-fluorobenzeneHCID 660424-CyanobenzaldehydeHCID 178418339Butyllithium

생성물 1

HCID 111837554-[(4-Fluorophenyl)(hydroxy)methyl]benzonitrile

시약·촉매·용매 3

HCID 8028Tetrahydrofuran용매2회
HCID 8058
Hexane
용매
HCID 8857Ethyl Acetate용매

실험 절차

5.00 g (28.57 mmol) of 4-fluorobromobenzene were dissolved in 100 ml tetrahydrofuran at −78° C. Addition of 21.4 ml (34.29 mmol) of a 1.6N solution of n-butyllithium in hexane was followed by stirring for 15 min and then dropwise addition of 4.50 g (34.29 mmol) of 4-cyanobenzaldehyde dissolved in 30 ml of tetrahydrofuran. The mixture was stirred at −78° C. for 1 h, warmed to RT and then stirred for 1 h. The reaction solution was mixed with water and ethyl acetate and the phases were separated. The aqueous phase was extracted three times with ethyl acetate, and the combined organic phases were washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the solid was filtered. The solvents were removed in vacuo and the crude product was purified by preparative HPLC (mobile phase: acetonitrile/water gradient). Acetonitrile was removed from the product-containing fractions in a rotary evaporator, and the aqueous residue was extracted with dichloromethane. Removal of the solvent resulted in 2.37 g (36% of theory) of the title compound.

후처리

  1. stirringThe mixture was stirred at −78° C. for 1 h
  2. stirringstirred for 1 h
  3. customthe phases were separated
  4. extractionThe aqueous phase was extracted three times with ethyl acetate
  5. washthe combined organic phases were washed with saturated aqueous sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. filtrationthe solid was filtered
  8. customThe solvents were removed in vacuo
  9. customthe crude product was purified by preparative HPLC (mobile phase: acetonitrile/water gradient)
  10. customAcetonitrile was removed from the product-containing fractions in a rotary evaporator
  11. extractionthe aqueous residue was extracted with dichloromethane
  12. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-61e703f27520421da663f803b99f0d84
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063234B2

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