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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034543Generated: October 31, 2026

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

https://huagongshe.com/reaction/1034543

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 numberUS08545877B2
Source datasetuspto-grants-2013_10
ORD IDord-7a9a6543c7a54595b60f0a16b7c2ff4d
Source noteuspto-grants-2013_10