HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perfluoro-1-butanesulfonyl fluoride → HCID 86674269, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86674268 | HCID 86674268 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86674269 | HCID 86674269 | — |
Reaction Steps
A 1.04 M THF solution of t-BuOK (4.9 mL, 5.1 mmol) was added to a 0° C., THF solution (4 mL) of 5-chloro-2-hydroxy-4-(trifluoromethyl)benzaldehyde (1.0 g, 4.6 mmol). After 4 min, neat 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride (1.7 mL, 9.3 mmol) was added and the ice bath was removed. After 1 h at room temperature, AcOH (1 mL) was added and the resulting mixture was concentrated. The resulting material was diluted with DCM and 1M aqueous HCl, the layers were separated, and the organic layer was washed with 1 M NaHCO3, dried (Na2SO4), and concentrated to yield the title compound that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748624B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-2201bf8f26e44e1790dc8ce1c220b374 |
| Source note | uspto-grants-2014_06 |