Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609483Generated: November 2, 2026

Imidazole → (S)-1-t-butyldimethylsilyloxy-2-triphenylmethylamino-3-(1-triphenylmethylimidazol-5-yl)propane

https://huagongshe.com/reaction/1609483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 15228563HCID 15228563—
SolventDimethylformamideHCID 6228—
Product(S)-1-t-butyldimethylsilyloxy-2-triphenylmethylamino-3-(1-triphenylmethylimidazol-5-yl)propaneHCID 15228564101.4%

Reaction Steps

Imidazole (12.269 g, 0.180 mol) and tert-butyldimethylsilyl chloride (TBDMSCl) (20.37 g, 0.135 mol) were added to a solution of the compound (XXI) (56.390 g, 0.0901 mol) in dry DMF (560 ml) under ice cooling, and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was poured into water, extracted with Et2O, washed with water and a saturated NaCl aqueous solution, then dried over Na2SO4, and concentrated to obtain a light-yellow foamy material (67.602 g). This crude product was purified by silica gel column chromatography (hexane/acetone=5/1) to obtain the objective compound (XX) (58.770 g; yield: 88.1%) as a white foamy material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401736
Source datasetuspto-grants-1995_03
ORD IDord-2526961bef8f4b44abc39114126f37a6
Source noteuspto-grants-1995_03