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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587999Generated: October 26, 2026

Hydrochloric Acid → (S)-3-[(R)-1-(2,4,5-Trifluorophenoxy)penyl]pyrrolidine

https://huagongshe.com/reaction/587999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDimethylformamideHCID 6228—
Reactant1,2,4,5-TetrafluorobenzeneHCID 9474—
ReactantSodium hydrideHCID 24758—
Reactant(S)-3-((R)-1-Hydroxypentyl)pyrrolidine-1-carboxylic acid t-butyl esterHCID 58104597—
Product(S)-3-[(R)-1-(2,4,5-Trifluorophenoxy)penyl]pyrrolidineHCID 131734426—

Reaction Conditions

Temperature90 °C

Reaction Steps

(S)-3-((R)-1-Hydroxypentyl)pyrrolidine-1-carboxylic acid t-butyl ester (40.0 mg, 155 μmol) was dissolved in DMF (100 mL, 12.9 mmol). While stirring, 60% sodium hydride in oil (0.4:0.6, sodium hydride:mineral oil, 18.6 mg, 311 μmol) was slowly added, and the mixture was stirred for 15 minutes. 1,2,4,5-Tetrafluorobenzene (52.1 μL, 466 μmol) was added. The mixture was then heated at 90° C. for 3 hours. The reaction was quenched with MeOH (1 mL), and the solvent was removed under reduced pressure. 1.25M HCl in EtOH (2.0 mL, 2.5 mmol) was added, and the mixture was stirred overnight. The product was concentrated and purified by preparative HPLC to yield the title compound as a mono-TFA salt (19.2 mg, 97% purity). MS m/z: [M+H]+ calcd for C15H20F3NO, 288.15. found 288.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227933B2
Source datasetuspto-grants-2016_01
ORD IDord-3d761ede706f44de9a5291bc2d04358e
Source noteuspto-grants-2016_01