Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581766Generated: October 31, 2026

Imidazole → 2-(tert-butyldiphenylsilyloxy)-N-methylethanamine

https://huagongshe.com/reaction/581766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-(Methylamino)ethanolHCID 8016—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(tert-butyldiphenylsilyloxy)-N-methylethanamineHCID 1182315831.1%

Reaction Steps

To a solution of N-methylethanolamine (600 mg), in N,N-dimethylformamide were added imidazole (1.13 g) and tert-butyldiphenylsilyl chloride (2.20 g) at ambient temperature with stirring. After 8 hours, the mixture was diluted with water (60 ml) and was extracted with ethyl acetate (20 ml) twice. The organic layer was washed with water three times and brine, dried over magnesium sulfate. The solvent was removed in vacuo. The residue was purified by column chromatography eluting with dichloromethane-methanol to give N-(2-tert-butyldiphenylsilyloxyethyl)-N-methylamine (780 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922711
Source datasetuspto-grants-1999_07
ORD IDord-c08107f503694a2ab70ecd180c89d8fe
Source noteuspto-grants-1999_07