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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920215Generated: November 2, 2026

Imidazole → HCID 59226436, compound

https://huagongshe.com/reaction/1920215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 59226607HCID 59226607—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 59226436HCID 5922643660%

Reaction Steps

To a solution of (+/−)-2-azido-4-(3-nitropyridin-4-yl)cyclohex-3-enol (1.0 equiv.) in DCM (0.15M) was added TBSCl (2.0 equiv.), imidazole (2.0 equiv.) and DMAP (0.1 equiv.) at room temperature. After 18 h, water was added, the organics were dried with brine, then Na2SO4, and concentrated. The crude material was loaded to silica gel and purified via ISCO eluting with ethyl acetate and hexanes (20%). Obtained (+/−)-4-(3-azido-4-(tert-butyldimethylsilyloxy)cyclohex-1-enyl)-3-nitropyridine as a yellow oil in 60% yield. LCMS (m/z): 376.3 (MH+), LC Rt=5.848 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168794B2
Source datasetuspto-grants-2012_05
ORD IDord-74b6f80635a7411ba43372876d9fd978
Source noteuspto-grants-2012_05