Benzene, 1-iodo-4-(trifluoromethyl)- → HCID 68822788, compound
Reaction equation
[CH2:1]([O:8][C:9](=[O:14])[CH2:10][CH2:11][C:12]#[CH:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.I[C:16]1[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=1>>[CH2:1]([O:8][C:9](=[O:14])[CH2:10][CH2:11][C:12]#[C:13][C:16]1[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
In analogy to the procedure described for example 8 a], pent-4-ynoic acid benzyl ester (Rosowsky, Andre; Forsch, Ronald A.; Queener, Sherry F., Journal of Medicinal Chemistry (2003), 46(9), 1726-1736) was reacted with 4-iodobenzotrifluoride in the presence of PdCl2(Ph3P)2 and cuprous iodide to give the title compound as yellow oil.
Sources & evidence
- ORD record
- ord-625768926b0d45b2adacf1eb69887c05
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405236B2
Reaction notes
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