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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977300Generated: October 31, 2026

Imidazole → HCID 11232313, compound

https://huagongshe.com/reaction/977300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDimethylformamideHCID 6228—
ProductHCID 11232313HCID 1123231392.3%

Reaction Steps

A solution of 1-(tert-butyloxycarbonyl)-4-piperidinol (5.2 g, 25.9 mmol), tert-butyldimethylsilyl chloride (4.07 g, 1.05 equiv.) and imidazole (2.7 g, 1.5 equiv.) in DMF (20 mL) was stirred for 16 h. After dilution with Et2O, the solution was washed successively with H2O (2×), 10% aqueous citric acid, a saturated aqueous solution of NaHCO3 and brine. The organic layer was dried (MgSO4) and concentrated to dryness. The residue was purified by HPLC using a WATERS® LC-500 preparative chromatography apparatus [2 SiO2 columns: hexane-EtOAc (19:1), Millipore Corporation, Milford, Mass., USA] to give 1-(tert-butyloxycarbonyl)-4-(tert-butyldimethylsiloxy)piperidine (7.54 g, 92%). 1H NMR (CDCl3) δ3.87 (m, 1H), 3.61 (ddd, J=3.5, 7.5, 13.0 Hz, 2H), 3.24 (ddd, J=3.7, 8.0, 13.0 Hz, 2H), 1.48 (s, 9H), 0.88 (s, 9H), 0.07 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614533
Source datasetuspto-grants-1997_03
ORD IDord-cd680aa462414f929c8b8d0f24b1c3aa
Source noteuspto-grants-1997_03