Water → HCID 19815306, compound
Reaction equation
[C:1]([C:3]1[CH:29]=[CH:28][CH:27]=[CH:26][C:4]=1[CH2:5][O:6][C:7]1[CH:25]=[CH:24][C:10]([CH2:11][N:12]2[C:16]([CH2:17][OH:18])=[C:15]([Cl:19])[N:14]=[C:13]2[CH2:20][CH2:21][CH2:22][CH3:23])=[CH:9][CH:8]=1)#[N:2].[CH3:30]C(C)([O-])C.[K+].CI.O>CS(C)=O>[C:1]([C:3]1[CH:29]=[CH:28][CH:27]=[CH:26][C:4]=1[CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:11][N:12]2[C:16]([CH2:17][O:18][CH3:30])=[C:15]([Cl:19])[N:14]=[C:13]2[CH2:20][CH2:21][CH2:22][CH3:23])=[CH:24][CH:25]=1)#[N:2]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 0.29 g of 1-[4-(2-cyanobenzyloxy)benzyl]-2-butyl-4-chloro-5-hydroxymethylimidazole in 8.0 mL of dimethyl sulfoxide at 25° was added 0.93 g of potassium t-butoxide followed by 0.060 mL of methyl iodide. The reaction mixture was stirred at 25° for 2.5 hours and then was poured into water. The aqueous emulsion was extracted with ethyl acetate; the organic phases were combined and washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Column chromatography on silica gel (elution: 5-25% ethyl acetate/benzene) furnished 0.17 g of 1-[4-(2-cyanobenzyloxy)benzyl]-2-butyl-4-chloro-5-methoxymethylimidazole; NWR (200 MHz, CDCl3): δ7.72-7.57 (m, 3H); 7.43 (m, 1H); 6.94 (s, 4h); 5.22 (s, 2H); 5.04 (s, 2H); 4.27 (s, 2H); 3.26 (s, 3H): 2.56 (t, 2H); 1.65 (quint., 2H); 1.33 (sext., 2H); 0.88 (t, 3H).
Workup
- extractionThe aqueous emulsion was extracted with ethyl acetate
- washwashed with water and brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-5c4c666e4b6540cfa70a77a757109746
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05128355
Reaction notes
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