HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373063Generated: October 31, 2026
Tert-butyl 3-oxopyrrolidine-1-carboxylate → HCID 23112167, compound
https://huagongshe.com/reaction/1373063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl 3-oxopyrrolidine-1-carboxylate | HCID 471360 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23112198 | HCID 23112198 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23112167 | HCID 23112167 | 64.1% |
Reaction Steps
A solution of Intermediate 1 (251 mg), and tert-butyl 3-oxo-1-pyrrolidinecarboxylate (563 mg, AstaTech) in dichloromethane (85 ml) was added with titanium tetraisopropoxide (905 μl, Aldrich) at room temperature, and stirred at room temperature for 19 hours. The reaction mixture was added with methanol (6 ml), and sodium borohydride (249 mg, Kanto Chemicals), and stirred at room temperature for 3.5 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (20 ml), and ethyl acetate (20 ml), and then the precipitates were removed by filtration. Then, the organic layer was separated, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1) to obtain the title compound (321 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160894B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-42ab8eda748e4e33a74fccb124bb2a84 |
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| Source note | uspto-grants-2007_01 |
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