Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454784Generated: October 25, 2026

Azidotrimethylsilane → {[3-Azido-4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}(triisopropyl)silane

https://huagongshe.com/reaction/1454784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidotrimethylsilaneHCID 78378—
ReactantIodosylbenzeneHCID 92125—
ReactantTriisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silaneHCID 67065786—
SolventDichloromethaneHCID 6344—
Product{[3-Azido-4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}(triisopropyl)silaneHCID 86616049—

Reaction Steps

In a three-neck flask, a stirred solution of triisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silane (26.06 g, 0.068 mol) in dichloromethane (260 mL) was cooled to −15° C. and treated with iodosobenzene (19.5 g, 0.089 mol) in four portions followed by azidotrimethylsilane (24 mL, 0.116 mol) while maintaining the temperature below −10° C. Stirring was continued for 1.5 h. The reaction mixture was allowed to warm to room temperature briefly, then cooled again back to −15° C. and filtered. The filtrate was evaporated under vacuum below 25° C. to give the title compound which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482336B2
Source datasetuspto-grants-2009_01
ORD IDord-c21e6395432d40d393ffc667993ee458
Source noteuspto-grants-2009_01