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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267174Generated: November 1, 2026

Iodine → HCID 22288240, compound

https://huagongshe.com/reaction/1267174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 11770078HCID 11770078—
SolventDichloromethaneHCID 6344—
ProductHCID 22288240HCID 22288240—

Reaction Conditions

Temperature7.5 °C

Reaction Steps

A solution of 5,7-dihydro-6H-dibenz[b,d]azepin-6-one (1.0 g, 4.77 mmol) (Example 3-A) and Et3N (2.66 mL, 19.12 mmol) was stirred for 5.0 minutes at −15° C. in CH2Cl2 and treated with TMSI (1.36 mL, 9.54 mmol). After stirring for 15 minutes I2 (1.81 g, 7.16 mmol) was added in a single portion and the reaction allowed to warm to 5-10° C. over 3 h. The reaction was quenched with sat. Na2SO3, diluted with CH2Cl2. and separated. The organics were washed with Na2SO3 and NaHSO3 and dried over MgSO4. After filtration, the organics were concentrated to approximately 20 mL and diluted with an additional 20 mL of hexanes. The title compound was isolated as a tan precipitate by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552013B1
Source datasetuspto-grants-2003_04
ORD IDord-930742a080734b228a24b5df68a39cf8
Source noteuspto-grants-2003_04