Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368758Generated: October 31, 2026

Imidazole → HCID 88230374, compound

https://huagongshe.com/reaction/1368758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2R-(t-Boc)amino-1,4-dichloro-3S-hydroxybutaneHCID 11368909—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 88230374HCID 8823037499.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 2(R)-(t-butyloxycarbonyl)amino-1,4-dichloro-3(S)-hydroxybutane (100.0 mg, 0.389 mmol) in dry DMF (2.5 mL) were added imidazole (79.4 mg, 1.67 mmol), DMAP (4.8 mg, 0.039 mmol) and TBS-Cl (175.9 mg, 1.167 mmol) at room temperature under N2. The resulting solution was stirred at 50° C. for 12 h. The reaction mixture was diluted with EtOAc (30 mL), washed with 0.1 N citric acid solution (5 mL), sat aqueous NaHCO3 (5 mL), water (5 mL) and brine (5 mL), dried over anhydrous magnesium sulfate, filtered, concentrated and column-chromatographed (10% EtOAc in n-Hex) to provide 2(S)-t-butyldimetylsilyloxy-3(R))-(t-butyloxycarbonyl)amino-1,4-dichlorobutane as a colorless solid (144.6 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573388B1
Source datasetuspto-grants-2003_06
ORD IDord-0980e191f96c40d78480699f635c26ef
Source noteuspto-grants-2003_06