Iodine → 3-Iodo-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-one
Reaction equation
[N+:1]([C:4]1[CH:15]=[CH:14][C:7]2[CH2:8][CH2:9][CH2:10][C:11](=[O:13])[NH:12][C:6]=2[CH:5]=1)([O-:3])=[O:2].CN(C)CCN(C)C.[I:24][Si](C)(C)C.II>C(Cl)Cl>[I:24][CH:10]1[C:11](=[O:13])[NH:12][C:6]2[CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:15]=[CH:14][C:7]=2[CH2:8][CH2:9]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -20 °C
Procedure
A mixture of 8-nitro-1,3,4,5-tetrahydro-1-benzazepin-2-one (1.72 g, 8.34 mmol) and N,N,N′,N′-Tetramethylethylenediamine (5.02 mL, 33.3 mmol) in methylene chloride (25 mL) was chilled to −20° C. and iodotrimethylsilane (5.32 g, 26.6 mmol) was added. The mixture became homogeneous and was stirred for 30 min before adding iodine (3.17 g, 12.5 mol). After stirring for 2 h at 0° C., the reaction was quenched with 10% aqueous Na2S2O3 and the mixture was filtered. The solid residue was washed with water (10×5 mL) and then with ether (2×2 mL) to yield 2.345 g of 3-iodo-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-one (contaminated with ˜8% starting material) that was used as such in the next reaction.
Workup
- stirringAfter stirring for 2 h at 0° C.
- customthe reaction was quenched with 10% aqueous Na2S2O3
- filtrationthe mixture was filtered
- washThe solid residue was washed with water (10×5 mL)
Sources & evidence
- ORD record
- ord-0c81d7110e7943e1aee531900177c68d
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08552186B2
Reaction notes
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