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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095671Generated: October 30, 2026

Imidazole → HCID 178455351, compound

https://huagongshe.com/reaction/2095671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDichloromethaneHCID 6344—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 178521568HCID 178521568—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 178455351HCID 178455351—

Reaction Steps

A mixture of trans-4-(4-iodo-1H-pyrazol-1-yl)cyclohexanol (1.00 g, 3.42 mmol), tert-butyldimethylsilyl chloride (1.03 g, 6.85 mmol), 4-dimethylaminopyridine (80 mg, 0.7 mmol), imidazole (699 mg, 10.3 mmol) and DCM (20 mL, 300 mmol) was stirred rt for 20 min. The material was transferred to a separatory funnel, extracting with DCM and sat. NaHCO3. The organic layer was dry-loaded onto silica gel for column chromatography, eluting with 3% EtOAc/hexanes. The fractions containing the pure product were concentrated in vacuo to afford the title compound as a clear oil. Typical yields are 95%. 1H NMR (400 MHz, DMSO-d6): δ=0.05 (s, 6H), 0.86 (s, 9H), 1.33-1.47 (m, 2H), 1.70-1.91 (m, 4H), 1.96 (d, J=11.9 Hz, 2H), 3.58-3.75 (m, 1H), 4.11-4.21 (m, 1H), 7.49 (s, 1H), 7.92 (s, 1H). MS (ES+): m/z=407.05 (100) [MH+]. HPLC: tR=3.22 min (v.v. non-polar—5 min, ZQ3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445510B2
Source datasetuspto-grants-2013_05
ORD IDord-561de1891da84623981539b8db2d3645
Source noteuspto-grants-2013_05