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Ethyl 3-(4-fluorophenyl)pentenoate → Ethyl 3-(4-fluorophenyl)valerate

HRID 362873
Notes
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Reaction equation

HRID 362873 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH2:15][CH3:16])=[CH:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][CH:3]=1.[H][H]>[Pd].C(O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([CH2:15][CH3:16])[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 54034845Ethyl 3-(4-fluorophenyl)pentenoateHCID 178418361HCID 178418361, compound

Product 1

HCID 23293610Ethyl 3-(4-fluorophenyl)valerateYield 126.8%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

A mixture of ethyl 3-(4-fluorophenyl)pentenoate (45.65 g,0.137 mol) and 10% palladium on carbon (0.86 g, Aldrich) in 95 % ethanol was shaken under 4 atm hydrogen pressure in a Parr hydrogenator for 1.5 hr. The mixture was filtered and concentrated by spin evaporation in vacuo. Fractional distillation gave 38.95 g (63%) of ethyl 3-(4-fluorophenyl)valerate as a clear oil contaminated with 29% triethyl phosphonoacetate. b.p., 133°-142° C. at 17 mm Hg;

Workup

  1. filtrationThe mixture was filtered
  2. concentrationconcentrated by spin evaporation in vacuo
  3. distillationFractional distillation

Sources & evidence

ORD record
ord-0ce4c0379cf745638e2122d217bd9ee6
Source dataset
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05872118

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes