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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133241Generated: October 27, 2026

Triethylamine → HCID 22288240, compound

https://huagongshe.com/reaction/133241

Reaction equation

Participants

RoleNameHCIDCharge
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 7-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 12 (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 numberUS07390801B2
Source datasetuspto-grants-2008_06
ORD IDord-fee94cde03f04cc18fa2fb4ccd7f9696
Source noteuspto-grants-2008_06