(Triphenylphosphoranylidene)acetaldehyde → (E)-3-[5-(3-Fluorophenyl)pyridin-2-yl]propenal
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[CH:10][C:11]([CH:14]=O)=[N:12][CH:13]=2)[CH:5]=[CH:6][CH:7]=1.C1(P(=[CH:35][CH:36]=[O:37])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>>[F:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[CH:10][C:11](/[CH:14]=[CH:35]/[CH:36]=[O:37])=[N:12][CH:13]=2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
584 mg of 5-(3-fluorophenyl)pyridine-2-carbaldehyde and 883 mg of (triphenylphosphoranylidene)acetaldehyde are stirred at RT overnight. The solvent is evaporated and the residue is purified by column chromatography (silica gel, MeOH:DCM=99.5:0.5).
Workup
- customThe solvent is evaporated
- customthe residue is purified by column chromatography (silica gel, MeOH:DCM=99.5:0.5)
Sources & evidence
- ORD record
- ord-7fe9c2ae255c46ebb809f0fbe1cb2bf1
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08791133B2
Reaction notes
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