Triethylamine → HCID 60029385, compound
Reaction equation
[C:1]([C:5]1[C:6]([O:16][CH:17]([CH3:19])[CH3:18])=[C:7]([C:10]([CH3:15])=[C:11]([C:13]#[CH:14])[CH:12]=1)[CH:8]=[O:9])([CH3:4])([CH3:3])[CH3:2].[CH3:20][O:21][C:22](=[O:31])[CH2:23][C:24]1[CH:29]=[CH:28][C:27](I)=[CH:26][CH:25]=1.C(N(CC)CC)C.C(OCC)(=O)C>CCCCCC.[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:20][O:21][C:22](=[O:31])[CH2:23][C:24]1[CH:25]=[CH:26][C:27]([C:14]#[C:13][C:11]2[CH:12]=[C:5]([C:1]([CH3:4])([CH3:2])[CH3:3])[C:6]([O:16][CH:17]([CH3:19])[CH3:18])=[C:7]([CH:8]=[O:9])[C:10]=2[CH3:15])=[CH:28][CH:29]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
Following General Procedure B and using 3-tert-butyl-5-ethynyl-2-isopropoxy-6-methyl-benzaldehyde (Intermediate 143, 0.35 g, 1.355 mmol), 4-iodo phenyl acetic acid methyl ester (0.374 g, 1.35 mmol), triethyl amine (8 mL), copper(I)iodide (0.02 g, 0.1 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.072 g, 0.1 mmol) followed by flash column chromatography over silica gel (230–400 mesh) using 3–5% ethyl acetate in hexane as the eluent, the title compound was obtained as a white solid (0.37 g, 75%).
Sources & evidence
- ORD record
- ord-9c89957bfe8147ebae6caf7ec5eb385f
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07226951B2
Reaction notes
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