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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161780Generated: October 29, 2026

Imidazole → HCID 59518835, compound

https://huagongshe.com/reaction/1161780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantN-(Benzyloxycarbonyl)-3-amino-1,2-propanediolHCID 3362144—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59518835HCID 59518835—

Reaction Steps

To a solution of benzyl 2,3-dihydroxypropylcarbamate in DMF (0.1 M) was added TBDMSCl (2.2 eq.) and imidazole (2.5 eq.) at room temperature. After stirred for 20 h, the reaction mixture was worked up with EtOAc, which was washed with water and brine. The organic layer was separated, dried and concentrated to give the crude bis-silylated product, which was dissolved in methanol (0.16 M) followed by addition of p-toluenesulfonic acid (0.1 equiv.) at 0° C. The reaction mixture was stirred for 1.5 h at the same temperature. After quenched with saturated NaHCO3 aqueous solution, the reaction mixture was extracted with EtOAc, which was washed with water and brine. The organic layer was separated, dried, concentrated, and purified on silica gel with 0-100% EtOAc/Hexanes gradient elution to provide the pure benzyl 2-(tert-butyldimethylsilyloxy)-3-hydroxypropylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820646B2
Source datasetuspto-grants-2010_10
ORD IDord-49c34ead2d654796aa40eca11fa8b9bb
Source noteuspto-grants-2010_10