Iodoethane → HCID 11543625, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:16])([F:15])[F:14])[C:8]=2[OH:17])[CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+].I[CH2:25][CH3:26]>C(#N)C>[CH2:25]([N:1]1[CH2:6][CH2:5][CH:4]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:15])([F:16])[F:14])[C:8]=2[OH:17])[CH2:3][CH2:2]1)[CH3:26]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Preparation according to Example 1: 2-piperidin-4-yl-6-(trifluoromethyl)phenol (0.01 g, 0.04 mmol), acetonitrile (2 ml), potassium carbonate (0.01 g) and iodoethane (0.01 ml). MS m/z (relative intensity, 70 eV) 273 (M+, 37), 259 (15), 258 (bp), 238 (18), 195 (19).
Workup
- customPreparation
Sources & evidence
- ORD record
- ord-d86c16eb89e44deaac65e26f69a8d7fa
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763639B2
Reaction notes
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