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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595966Generated: October 31, 2026

Perfluoro-1-butanesulfonyl fluoride → HCID 118045501, compound

https://huagongshe.com/reaction/595966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantDiisopropylethylamineHCID 81531—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
ReactantHCID 11032835HCID 11032835—
Solvent(Trifluoromethyl)benzeneHCID 7368—
ProductHCID 118045501HCID 11804550130%

Reaction Steps

To a solution of (S)-2-(2-hydroxy-1-phenylethyl)isoindoline-1,3-dione (1.5 g, 5.61 mmol) in PhCF3 (18.71 mL) was added triethylamine trihydrofluoride (5.48 mL, 33.7 mmol), perfluorobutanesulfonyl fluoride (1.019 mL, 5.67 mmol), DIEA (14.70 mL, 84 mmol) at room temperature. The reaction mixture was stirred at room temperature for 1 h, then more perfluorobutanesulfonyl fluoride (1.019 mL, 5.67 mmol) was added. After 5 h, the reaction mixture was quenched with NaHCO3 and extracted with EtOAc. The combined organic layers were washed with water and brine, dried over anhydrous sodium sulfate, filtered off, and concentrated in vacuo. The crude product was purified by flash chromatography (0-10% EtOAC in heptane) yielding (S)-2-(2-fluoro-1-phenylethyl)isoindoline-1,3-dione (30% yield). LCMS (m/z): 270.1 (MH+), 0.96 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-ea4caffecdc04c22826c17e1a1919dbf
Source noteuspto-grants-2016_01