HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108808Generated: October 31, 2026
Perfluorooctanesulfonyl fluoride → HCID 66704853, compound
https://huagongshe.com/reaction/2108808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perfluorooctanesulfonyl fluoride | HCID 9388 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 66704846 | HCID 66704846 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66704853 | HCID 66704853 | — |
Reaction Steps
Process B: (3S,4R)-3-Bromomethyl-1-tert-butoxycarbonyl-4-hydroxypyrrolidine (561 mg) was dissolved in toluene (20 mL). To this solution, 1,8-diazabicyclo[5.4.0]undec-7-ene (0.50 mL) was added and perfluoro-1-octanesulfonylfluoride (0.93 mL) was then added dropwise while the mixture was chilled in an ice water bath. After stirred at 2° C. for 1 hour, the reaction mixture was poured on a silica gel pad and was eluted with ethyl acetate (100 mL). The eluate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluant: hexane: ethyl acetate=2:1) to give (3S,4S)-3-bromomethyl-1-tert-butoxycarbonyl-4-fluoropyrrolidine as a yellow oil (447 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514451B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-0d6dc8abee5a46a9bc98d451e9ec3184 |
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| Source note | uspto-grants-2009_04 |
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