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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N,N-Diethylethanamine trihydrofluoride | HCID 175505 | — |
| Reactant | HCID 11032835 | HCID 11032835 | — |
| Solvent | (Trifluoromethyl)benzene | HCID 7368 | — |
| Product | HCID 118045501 | HCID 118045501 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-ea4caffecdc04c22826c17e1a1919dbf |
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| Source note | uspto-grants-2016_01 |
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