HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(tert-butyl)-5-cyanofuran-2-sulfonamide → 5-Cyanofuran-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(tert-butyl)-5-cyanofuran-2-sulfonamide | HCID 53628367 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-Cyanofuran-2-sulfonamide | HCID 53628369 | — |
Reaction Steps
A solution of N-(tert-butyl)-5-cyanofuran-2-sulfonamide (the product of example 50, step i) (1.0 g) in trifluoroacetic acid (30 mL) was stirred at room temperature for 24 h. The mixture was evaporated to dryness in vacuo to leave a crude yellow oil that was triturated with Et2O and filtered. The filtrate was evaporated to dryness in vacuo to give the subtitle compound as a pale yellow oil. Yield: 0.29 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410123B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-894719ac065240739e6c5ce47c677327 |
| Source note | uspto-grants-2013_04 |