Azobisisobutyronitrile → HCID 22103390, compound
Reaction equation
[CH3:1][N:2]1[N:6]=[N:5][C:4]([C:7]2[CH:33]=[C:32]([CH3:34])[C:10]([O:11][CH2:12][CH2:13][CH2:14][CH:15]([C:26]3[N:27]([CH3:31])[CH:28]=[CH:29][N:30]=3)OC(OC3C=CC=CC=3)=S)=[C:9]([CH3:35])[CH:8]=2)=[N:3]1.CC(N=NC(C#N)(C)C)(C#N)C.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[CH3:1][N:2]1[N:6]=[N:5][C:4]([C:7]2[CH:33]=[C:32]([CH3:34])[C:10]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][C:26]3[N:27]([CH3:31])[CH:28]=[CH:29][N:30]=3)=[C:9]([CH3:35])[CH:8]=2)=[N:3]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-[4-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-1-phenoxythiocarbonyloxy-butyl]-1-methylimidazole (1.94 mmol) in 35 ml of toluene was added AIBN (159 mg, 0.97 mmol) and n-tributyltin hydride (1.69 g), and the mixture was stirred at 75°-80° C. for 4 h. An aqueous sodium bicarbonate solution was added to the mixture, and the mixture was extracted with ethyl acetate, and then methylene chloride (2×). The combined organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica column chromatography (20 cm column, methylene chloride/methanol, 30/1-15/1) to afford 440 mg (67%) of 2-[4-[4-(2-methyltetrazol-5-yl)-2,6-dimethylphenoxy]-butyl]-1-methylimidazole, m.p. 100°-102° C. (from methylene chloride/hexane).
Workup
- extractionthe mixture was extracted with ethyl acetate
- dry with materialThe combined organic layer was dried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified by silica column chromatography (20 cm column, methylene chloride/methanol, 30/1-15/1)
Sources & evidence
- ORD record
- ord-2b03efc196af4f56aa35a0547e5504ee
- Source dataset
- uspto-grants-1998_12
- Patent number
- US05846986
Reaction notes
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