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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202259Generated: November 2, 2026

Imidazole → Ethyl trans-2-((tert-butyldiphenylsilyloxy)methyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/2202259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant(1R,2R)-2-(ethoxycarbonyl)cyclopropane-1-carboxylic acidHCID 11535603—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl trans-2-((tert-butyldiphenylsilyloxy)methyl)cyclopropanecarboxylateHCID 13173573779%

Reaction Steps

1M Borane-THF complex THF solution (85 mL, 84.98 mmol) was added to a solution of trans-2-(ethoxycarbonyl)cyclopropanecarboxylic acid (11.2 g, 70.82 mmol) in THF (100 mL) at 0° C., and the mixture was stirred overnight at room temperature. MeOH was added thereto, and then the gas was not generated. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in DMF (50 mL), tert-butylchlorodiphenylsilane (20.10 mL, 84.98 mmol) and imidazole (5.79 g, 84.98 mmol) were added thereto, and the mixture was stirred for 5 hr. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate, and concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (solvent gradient; 2→35% ethyl acetate/hexane) to give ethyl trans-2-((tert-butyldiphenylsilyloxy)methyl)cyclopropanecarboxylate (21.40 g, 55.9 mmol, 79%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-16305b4412bc4d2a9013982d402d7493
Source noteuspto-grants-2016_06