HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perfluoro-1-butanesulfonyl fluoride → HCID 57927655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 11729567 | HCID 11729567 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57927655 | HCID 57927655 | — |
Reaction Steps
After dissolving (R)-1-benzyloxy-3-trityloxypropan-2-ol (CAS 83526-68-5) (10.45 g) in toluene (50 ml), nonafluoro-1-butanesulfonyl fluoride (7.95 ml) was added and the mixture was cooled on ice. Next, 1,8-diazabicyclo[5.4.0]undeca-7-ene (6.63 ml) was added dropwise while stirring. The mixture was stirred for 30 minutes on ice, and then for 3 hours and 30 minutes at room temperature. The reaction mixture was directly purified by silica gel column chromatography to obtain the title compound (7.52 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252810B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-48bf30a3c8614c3db69385e99933b98b |
| Source note | uspto-grants-2012_08 |