HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041496Generated: November 1, 2026
Iodine → 3-Iodo-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-one
https://huagongshe.com/reaction/1041496
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 8-Nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one | HCID 4093214 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Iodo-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-one | HCID 67263430 | 84.7% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552186B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0c81d7110e7943e1aee531900177c68d |
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| Source note | uspto-grants-2013_10 |
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