HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399398Generated: October 31, 2026
HCID 22855968, compound → HCID 10621099, compound
https://huagongshe.com/reaction/2399398
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22855968 | HCID 22855968 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10621099 | HCID 10621099 | 78% |
Reaction Steps
To a solution of (2R,4R)-N-tert-butoxycarbonyl-4-tert-butyldimethylsiloxy-2-[(E)-2-ethoxycarbonylvinyl]-pyrrolidine (20 g, 50 mmol) in ethanol (500 ml) was added 10% palladium-carbon (5 g), and the mixture was stirred under atmospheric pressure in a hydrogen atmosphere at room temperature for 2 h. Further, 10% palladium-carbon (2 g) was added thereto, and the mixture was stirred under atmospheric pressure in a hydrogen atmosphere at room temperature for 1.5 h. The catalyst was filtered off, and the solvent was removed in vacuo. The residue was subjected to silica gel column chromatography (Wakogel™ C-300, heptane-ethyl acetate) to give (2R,4R)-N-tert-butoxycarbonyl-4-tert-butyldimethylsiloxy-2-(2-ethoxycarbonylethyl)pyrrolidine (15.62 g, yield: 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05449672 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-c9ce553da4bf4d5baafebd220d009cb1 |
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| Source note | uspto-grants-1995_09 |
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