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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270108Generated: October 30, 2026

Tert-butyl 3-oxopyrrolidine-1-carboxylate → Tert-butyl 3-hydroxy-3-(trifluoromethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/270108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-hydroxy-3-(trifluoromethyl)pyrrolidine-1-carboxylateHCID 50986427—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl 3-oxopyrrolidine-1-carboxylate (926 mg, 5.0 mmol) was dissolved in THF (10 mL) and the solution was cooled to 0° C., trimethyl(trifluoromethyl)silane (0.872 mL) and tetrabutylammonium fluoride (TBAF) (176 mg, 0.557 mmol) were added. The ice-bath was removed and the reaction mixture was stirred at room temperature overnight. Saturated aqueous NH4Cl solution (8 mL) was added and stirring was continued. After 15 min TBAF (2.36 g TBAF in 7.5 mL THF) was added and the reaction mixture was stirred at room temperature for 1 h. The reaction mixture was extracted with ethyl acetate, washed with H2O, dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (0-40% ethyl acetate in petroleum spirit) to give the subtitled compound (800 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449475B2
Source datasetuspto-grants-2008_11
ORD IDord-a6b254a7963647e2a0a6eee234177e7a
Source noteuspto-grants-2008_11