Iodine → HCID 53739951, compound
Reaction equation
II.I[CH2:4]I.[C:6]([C:8]1[CH:13]=[CH:12][C:11]([C:14]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=2)=[CH2:15])=[CH:10][CH:9]=1)#[N:7]>C1(C)C=CC=CC=1.[Cu]>[Cl:22][C:19]1[CH:18]=[CH:17][C:16]([C:14]2([C:11]3[CH:10]=[CH:9][C:8]([C:6]#[N:7])=[CH:13][CH:12]=3)[CH2:4][CH2:15]2)=[CH:21][CH:20]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
600 mg of Copper powder are cauterized with 10 mg of iodine in 10 ml of toluene. 1.2 g of Diiodomethane and 500 mg of 1-(4-cyanophenyl)-1-(4-chlorophenyl)-ethylene are added and the mixture refluxed for 140 hours and then filtered and the filtrate concentrated. The oily residue is chromatographed on silica gel with toluene as eluant.
Workup
- temperaturethe mixture refluxed for 140 hours
- filtrationfiltered
- concentrationthe filtrate concentrated
- customThe oily residue is chromatographed on silica gel with toluene as eluant
Sources & evidence
- ORD record
- ord-cb5f4a7023b642f0ac9b743926db2342
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05112851
Reaction notes
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