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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | (1R,2R)-2-(ethoxycarbonyl)cyclopropane-1-carboxylic acid | HCID 11535603 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl trans-2-((tert-butyldiphenylsilyloxy)methyl)cyclopropanecarboxylate | HCID 131735737 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365520B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-16305b4412bc4d2a9013982d402d7493 |
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| Source note | uspto-grants-2016_06 |
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