HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588121Generated: October 30, 2026
2,2-Difluoro-2-(fluorosulfonyl)acetic acid → HCID 118168965, compound
https://huagongshe.com/reaction/588121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Difluoro-2-(fluorosulfonyl)acetic acid | HCID 2737516 | — |
| Reactant | HCID 11032835 | HCID 11032835 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118168965 | HCID 118168965 | — |
Reaction Steps
(S)-2-(2-hydroxy-1-phenylethyl)isoindoline-1,3-dione (1.06 g, 3.97 mmol) was dissolved in anhydrous acetonitrile (20 ml), charged with copper (I) iodide (1.133 g, 5.95 mmol), 2,2-difluoro-2-(fluorosulfonyl)acetic acid (0.615 ml, 5.95 mmol), degassed under nitrogen and heated to 80° C. The solution was allowed to stir at 80° C. for 1 hr. The reaction was cooled in an ice bath, quenched with 5 mL water, filtered through a 10 g celite cartridge, and the solvents were removed in vacuo. The residue was purified by MPLC 10-50% EtOAc/hexanes to provide (S)-2-(2-(difluoromethoxy)-1-phenylethyl)isoindoline-1,3-dione. MS: [M+H]+ m/z 318.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09226922B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-be8d548f4dda4c95b2563d6946584079 |
|---|
| Source note | uspto-grants-2016_01 |
|---|