HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606724Generated: October 31, 2026
Water → (2S)-1-[2-(benzenesulfonyloxy)acetyl]-4,4-difluoropyrrolidine-2-carbonitrile
https://huagongshe.com/reaction/606724
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | (2S)-1-[2-(benzenesulfonyloxy)acetyl]-4,4-difluoropyrrolidine-2-carboxamide | HCID 24781878 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2S)-1-[2-(benzenesulfonyloxy)acetyl]-4,4-difluoropyrrolidine-2-carbonitrile | HCID 24781879 | 96% |
Reaction Steps
(2S)-1-[2-(benzenesulfonyloxy)acetyl]-4,4-difluoropyrroli dine-2-carboxamide (872 mg) was dissolved in acetonitrile (16 mL), followed by triethylamine (1.05 mL). While this mixture was cooled in a salt-ice bath, trifluoroacetic anhydride (0.53 mL) was added dropwise. The mixture was stirred at the same temperature for 1 hour, followed by the addition of water (16 mL) and extraction with ethyl acetate (2×60 mL). The ethyl acetate extracts were combined, washed with saturated brine (2×20 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified on a silica gel column (eluant=hexane:ethyl acetate=1:1) to give (2S)-1-[2-(benzenesulfonyloxy)acetyl]-4,4-difluoropyrrolidine-2-carbonitrile as a white crystal (789 mg, 96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07915427B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-1b01ef1ba74d4163b1d092f1cf0e6c32 |
|---|
| Source note | uspto-grants-2011_03 |
|---|