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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895915Generated: November 1, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/1895915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(S)-3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 59704735—
ProductTrifluoroacetic acidHCID 6422242.9%
Product(S)-2-(pyrrolidin-3-yloxy)isoindoline-1,3-dioneHCID 67118875—

Reaction Steps

Trifluoroacetic acid (3.42 g, 30.0 mmol) was added to a solution of (S)-tert-butyl 3-(1,3-dioxoisoindolin-2-yloxy)pyrrolidin-1-carboxylate (3.32 g, 10.0 mmol) CH2Cl2 (25 ml) at 0° C. The reaction mixture was stirred at room temperature for 17 hours and concentrated in vacuo. The residue was triturated with diethyl ether (100 ml) to give (S)-2-(pyrrolidin-3-yloxy)isoindoline-1,3-dione)trifluoroacetic acid salt (2.77 g, 80%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518934B2
Source datasetuspto-grants-2013_08
ORD IDord-bd1637c156fc47bc874334d0178c2d86
Source noteuspto-grants-2013_08