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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121495Generated: November 3, 2026

Iodine → HCID 22288240, compound

https://huagongshe.com/reaction/2121495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant8-Azatricyclo[9.4.0.0,2,7]pentadeca-1(15),2,4,6,11,13-hexaen-9-oneHCID 11367798—
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) were 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 numberUS06696438B2
Source datasetuspto-grants-2004_02
ORD IDord-ea9fa7c370274fad8f2cc50c0b89ab1d
Source noteuspto-grants-2004_02