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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186356Generated: October 26, 2026

(Trifluoromethyl)trimethylsilane → 2-(Pyrrolidin-1-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridine

https://huagongshe.com/reaction/1186356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant6-(Pyrrolidin-1-yl)pyridine-3-carbaldehydeHCID 2794775—
SolventTetrahydrofuranHCID 8028—
Product2-(Pyrrolidin-1-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridineHCID 6740173694%

Reaction Steps

According to Reference Example 8-12, by use of 6-(pyrrolidin-1-yl)-3-pyridinecarboxaldehyde (173 mg, 0.982 mmol), (trifluoromethyl)trimethylsilane (174 μL, 1.18 mmol), tetrabutylammonium fluoride (a 1.0 mol/L solution in tetrahydrofuran, 98.0 μL, 0.098 mmol) and tetrahydrofuran (5.0 mL), the mixture was stirred and reacted at room temperature for 30 minutes. Then, slurry purification was performed using hexane, to give 2-(pyrrolidin-1-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridine (Compound DH) (227 mg, yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673908B2
Source datasetuspto-grants-2014_03
ORD IDord-fd9eef4168e448158e86ec565aff527f
Source noteuspto-grants-2014_03