HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-t-butyl-3-benzoyloxy-1-pentanesulfonamide → HCID 18467564, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-t-butyl-3-benzoyloxy-1-pentanesulfonamide | HCID 18467574 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 18467564 | HCID 18467564 | 80.9% |
Reaction Steps
A mixture of N-t-butyl-3-benzoyloxy-1-pentanesulfonamide (90.4 g) and trifluoroacetic acid (200 ml) was stirred overnight at room temperature. Trifluoroacetic acid was removed under reduced pressure and water and chloroform were added to the residue. A saturated aqueous solution of sodium hydrogencarbonate was added thereto with vigorously stirring until the aqueous layer became neutral. After extraction with chloroform, the organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate=2/1 to 1/1) to obtain 3-benzoyloxy-1-pentanesulfonamide (60.6 g) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420409B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-3249c274d15d48eaa429edd69d475f15 |
| Source note | uspto-grants-2002_07 |