Tetrahydrofuran → HCID 86730620, compound
Reaction equation
CO[C:3]1[CH:10]=[C:9]([C:11]#[C:12][Si:13]([CH:20]([CH3:22])[CH3:21])([CH:17]([CH3:19])[CH3:18])[CH:14]([CH3:16])[CH3:15])[C:8]([O:23][CH2:24][CH3:25])=[CH:7][C:4]=1[CH:5]=O.[CH2:26]([O:28][C:29]1[CH:43]=[C:42]([I:44])[C:41]([O:45][CH3:46])=[CH:40][C:30]=1[CH2:31]P(=O)(OCC)OCC)[CH3:27].[H-].[Na+].O1CCC[CH2:50]1>>[CH2:26]([O:28][C:29]1[CH:43]=[C:42]([I:44])[C:41]([O:45][CH3:46])=[CH:40][C:30]=1[CH:31]=[CH:5][C:4]1[C:3]([CH3:50])=[CH:10][C:9]([C:11]#[C:12][Si:13]([CH:14]([CH3:16])[CH3:15])([CH:20]([CH3:22])[CH3:21])[CH:17]([CH3:19])[CH3:18])=[C:8]([O:23][CH2:24][CH3:25])[CH:7]=1)[CH3:27]Participants
5
Procedure
The 2-methoxy-5-ethoxy-4-((tri-iso-propylsilyl)ethynyl)benzaldehyde and diethyl 2-ethoxy-4-iodo-5-methoxybenzylphosphonate can be added to a solution containing sodium hydride (NaH) dissolved in tetrahydrofuran (THF), yielding (E)-((4-(2-ethoxy-4-iodo-5-methoxystyryl)-(2-ethoxy-5-methylphenyl)ethynyl)tri-iso-propylsilane.
Sources & evidence
- ORD record
- ord-fa182a0eb71a4992867dc6ee7b367b11
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937148B2
Reaction notes
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