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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant8-Nitro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 4093214—
SolventDichloromethaneHCID 6344—
Product3-Iodo-8-nitro-1,3,4,5-tetrahydro-benzo[b]azepin-2-oneHCID 6726343084.7%

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-0c81d7110e7943e1aee531900177c68d
Source noteuspto-grants-2013_10