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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045261Generated: October 29, 2026

Imidazole → 1-(t-Butyldimethylsilyloxy)-3-dimethylamino-2-propanol

https://huagongshe.com/reaction/1045261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-(Dimethylamino)-1,2-propanediolHCID 79078—
SolventDichloromethaneHCID 6344—
Product1-(t-Butyldimethylsilyloxy)-3-dimethylamino-2-propanolHCID 86617949—

Reaction Conditions

Temperature0 °C

Reaction Steps

A dry dichloromethane (10 mL) solution of 3-(dimethylamino)-1,2-propanediol (98%, 1.00 g, 8.39 mmol, 1.0 equiv) and imidazole (0.57 g, 8.39 mmol, 1.0 equiv) was stirred at 0° C. under argon for 15 minutes. Solid tert-butyldimethylsilyl chloride (1.26 g, 8.39 mmol, 1.0 equiv) was added to the mixture and the resultant was stirred for 2 hours at 0° C. The mixture was then diluted with 20 mL of dichloromethane and poured into deionized water (15 mL). The organic layer was separated and the aqueous layer was extracted with two additional portions of dichloromethane (20 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated to afford crude 1-(tert-butyldimethylsilyloxy)-3-(dimethylamino)propan-2-ol, a thick clear oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08568772B2
Source datasetuspto-grants-2013_10
ORD IDord-2a06376faa984a30989d5d1af561974a
Source noteuspto-grants-2013_10