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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671378Generated: October 26, 2026

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

https://huagongshe.com/reaction/1671378

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)pentyl]pyrrolidineHCID 58104617—

Reaction Conditions

Temperature90 °C

Reaction Steps

(S)-3-((R)-1-Hydroxypentyl)pyrrolidine-1-carboxylic acid t-butyl ester (40.0 mg, 155 μmmol) 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 μmmol) was slowly added, and the mixture was stirred for 15 minutes. 1,2,4,5-Tetrafluorobenzene (52.1 μL, 466 μmmol) 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 numberUS07994209B2
Source datasetuspto-grants-2011_08
ORD IDord-7484aea67ff1420eb6a0bba6e22a6750
Source noteuspto-grants-2011_08