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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23112198HCID 23112198—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 23112167HCID 2311216764.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160894B2
Source datasetuspto-grants-2007_01
ORD IDord-42ab8eda748e4e33a74fccb124bb2a84
Source noteuspto-grants-2007_01