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Ethyl Acetate → (e)-3-(4-Iodophenyl)-3-(3-trifluoromethylphenyl)prop-2-en-1-ol

HRID 549866
Notes
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Reaction equation

HRID 549866 reaction equation
C[O-].[Na+].[H-].[Al+3].[Li+].[H-].[H-].[H-].[F:10][C:11]([F:23])([F:22])[C:12]1[CH:13]=[C:14]([C:18]#[C:19][CH2:20][OH:21])[CH:15]=[CH:16][CH:17]=1.C(OCC)(=O)C.[I:30][C:31]1[CH:36]=[CH:35][C:34](I)=[CH:33][CH:32]=1.O1C=CC=C1P(C1OC=CC=1)C1OC=CC=1>O1CCCC1.[Cl-].[Zn+2].[Cl-]>[I:30][C:31]1[CH:36]=[CH:35][C:34](/[C:18](/[C:14]2[CH:15]=[CH:16][CH:17]=[C:12]([C:11]([F:22])([F:23])[F:10])[CH:13]=2)=[CH:19]\[CH2:20][OH:21])=[CH:33][CH:32]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

9

Reactant 6

HCID 8857Ethyl AcetateHCID 12208p-DiiodobenzeneHCID 521585Tris(furan-2-yl)phosphaneHCID 10942334Sodium MethoxideHCID 21226445Aluminium lithium hydrideHCID 227309473-(3-(Trifluoromethyl)phenyl)prop-2-yn-1-ol

Product 1

HCID 19261273
(e)-3-(4-Iodophenyl)-3-(3-trifluoromethylphenyl)prop-2-en-1-ol

Reagents, catalysts & solvents 2

HCID 3007855ZincchlorideCatalystHCID 8028TetrahydrofuranSolvent3×

Conditions

Temperature
0 °C

Procedure

Sodium methoxide (90 mg, 1.67 mmol) was added to 1 M solution of lithium aluminum hydride in tetrahydrofuran (33 mL, 33 mmol) under argon. The mixture was cooled to 0° C. and a solution of the above alcohol (6.7 g, 33.5 mmol) in tetrahydrofuran (25 mL) was added over 10 min. The reaction was stirred at 0° C. for 3 h; dry ethyl acetate (10 mL, 103 mmol) was added and the whole mixture was stirred at ambient temperature for 15 min. A degassed solution of 1,4-diiodobenzene (13.25 g, 40.1 mmol) in dry tetrahydrofuran (25 mL), anhydrous zinc chloride (2.73 g, 20.0 mmol), tris(dibenzylideneacetone)dipalladium chloroform complex (0.692 g, 0.66 mmol), and tri(2-furyl)phosphine (0.854 g, 3.6 mmol) were added; the mixture was degassed and then was heated at 60° C. for 15 h under argon. The suspension was cooled down; methanol (16 mL) was added and the mixture was stirred for additional 1 h. The reaction was diluted with ether (350 mL) and saturated aqueous solution of ammonium chloride (9 mL) was added. The mixture was filtered through a paddle of silica gel and the paddle was thoroughly washed with ether (100 mL). The solvents were evaporated in vacuo and the residue was purified by flash column chromatography (silica gel Fluka 60, hexanes/ethyl acetate 5:1) affording (E)-3-(4-iodophenyl)-3-(3-trifluoromethylphenyl)prop-2-en-1-ol as solidifying oil.

Workup

  1. stirringthe whole mixture was stirred at ambient temperature for 15 min
  2. customthe mixture was degassed
  3. temperaturewas heated at 60° C. for 15 h under argon
  4. temperatureThe suspension was cooled down
  5. additionmethanol (16 mL) was added
  6. stirringthe mixture was stirred for additional 1 h
  7. additionThe reaction was diluted with ether (350 mL) and saturated aqueous solution of ammonium chloride (9 mL)
  8. additionwas added
  9. filtrationThe mixture was filtered through a paddle of silica gel
  10. washthe paddle was thoroughly washed with ether (100 mL)
  11. customThe solvents were evaporated in vacuo
  12. customthe residue was purified by flash column chromatography (silica gel Fluka 60, hexanes/ethyl acetate 5:1)

Sources & evidence

ORD record
ord-15846b8eca67457da4617f51b6b3e5b5
Source dataset
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07943613B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes