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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221010Generated: November 1, 2026

Imidazole → HCID 59710103, compound

https://huagongshe.com/reaction/2221010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 59710385HCID 59710385—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 59710103HCID 5971010388.4%

Reaction Steps

1-(1,1-dimethylethyl) 2-ethyl(2S,3S)-3-hydroxy-1,2-pyrrolidinedicarboxylate (8.98 g, 34.7 mmol), imidazole (2.36 g, 34.7 mmol), dimethylaminopyridine (50 mg, catalytic) and chloro(1,1-dimethylethyl)dimethylsilane (4.96 g, 32.9 mmol) were stirred at room temperature for 16 hours. The reaction was diluted with water and 1N HCl to make the mixture acidic. The mixture was extracted three times with methylene chloride. The organic layer was washed with 1M HCl, dried over MgSO4 to give the title compound as a clear brown oil (10.88 g, 29.1 mmol). 1H NMR (400 MHz, DMSO-D6) δ ppm 0.0 (m, 6 H) 0.8 (m, 9 H) 1.2 (m, 3 H) 1.3 (m, 9 H) 1.7 (m, 1 H) 1.9 (m, 1 H) 3.4 (m, 2 H) 3.9 (m, 1 H) 4.1 (m, 2 H) 4.4 (m, 1 H). ES+=374.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368453B2
Source datasetuspto-grants-2008_05
ORD IDord-e4ceb892cbf844a2b723d1b269a6fa1d
Source noteuspto-grants-2008_05