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2-(4-Trifluoromethyl-phenyl)-pyrimidine-5-carbaldehyde → Cyclopentyl(2-(4-(trifluoromethyl)phenyl)pyrimidin-5-yl)methanol

HRID 2407026
Notes
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Reaction equation

HRID 2407026 reaction equation
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:14]=[CH:13][C:12]([CH:15]=[O:16])=[CH:11][N:10]=2)=[CH:5][CH:4]=1.[CH:19]1([Mg]Br)[CH2:23][CH2:22][CH2:21][CH2:20]1>C1COCC1>[CH:19]1([CH:15]([C:12]2[CH:13]=[N:14][C:9]([C:6]3[CH:5]=[CH:4][C:3]([C:2]([F:1])([F:17])[F:18])=[CH:8][CH:7]=3)=[N:10][CH:11]=2)[OH:16])[CH2:23][CH2:22][CH2:21][CH2:20]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 219363042-(4-Trifluoromethyl-phenyl)-pyrimidine-5-carbaldehydeHCID 178419650HCID 178419650, compound

Product 1

HCID 67980743Cyclopentyl(2-(4-(trifluoromethyl)phenyl)pyrimidin-5-yl)methanol

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
0 °C

Procedure

To a −78° C. solution of 2-(4-(trifluoromethyl)phenyl)pyrimidine-5-carbaldehyde (1.0 g, 3.96 mmol) in THF (6 mL) was added cyclopentylmagnesium bromide (2.97 mL of a 2.0M solution in THF, 5.95 mmol). The solution was stirred at 0° C. for two hours. The mixture was quenched with saturated aqueous NH4Cl, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude residue was purified by silica gel chromatography to give cyclopentyl(2-(4-(trifluoromethyl)phenyl)pyrimidin-5-yl)methanol (1.0 g) as a red oil.

Workup

  1. customThe mixture was quenched with saturated aqueous NH4Cl
  2. dry with materialdried over anhydrous Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe crude residue was purified by silica gel chromatography

Sources & evidence

ORD record
ord-bfd18e26e9634150a5bcaa7bad5ea5ab
Source dataset
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08809342B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes