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ethyl (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-ynoate → (E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-ol

HRID 379955
Notes
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Reaction equation

HRID 379955 reaction equation
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:8]=[CH:7][C:6]([C:9]#[C:10]/[CH:11]=[CH:12]/[C:13](OCC)=[O:14])=[CH:5][CH:4]=1.[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1>C1(C)C=CC=CC=1>[F:1][C:2]([F:18])([F:19])[C:3]1[CH:4]=[CH:5][C:6]([C:9]#[C:10]/[CH:11]=[CH:12]/[CH2:13][OH:14])=[CH:7][CH:8]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 20693054ethyl (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-ynoateHCID 86583787Diisobutylaluminumhydride toluene

Product 1

HCID 18363296(E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-olYield 87.2%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Conditions

Temperature
0 °C

Procedure

In 4 ml of toluene were dissolved 480 mg (1.79 mmol) of ethyl (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-ynoate, and 2.38 ml (3.58 mmol) of a 1.5M diisobutyl aluminum hydride-toluene solution were added to the solution with stirring at 0° C. After 10 minutes, ice was added to the mixture and the insolubles were removed by filtration using Celite. After the organic layer was dried, the crude product obtained by evaporation of the solvent was subjected to column chromatography using 15 g of silica gel and eluted with a mixed solvent of ethyl acetate-hexane (3:17) to obtain 353 mg (yield: 87%) of the title compound as an oil.

Workup

  1. additionwere added to the solution
  2. additionice was added to the mixture
  3. customthe insolubles were removed by filtration
  4. customAfter the organic layer was dried
  5. customthe crude product obtained by evaporation of the solvent
  6. washeluted with a mixed solvent of ethyl acetate-hexane (3:17)

Sources & evidence

ORD record
ord-3c0d32b591254132be54c65fe4804522
Source dataset
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06300357B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes