HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl iodide → N-(tert-Butyl)-5-isobutylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | 5-Butyl-N-tert-butylthiophene-2-sulfonamide | HCID 11993904 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(tert-Butyl)-5-isobutylthiophene-2-sulfonamide | HCID 11482758 | — |
Reaction Steps
The titled compound was prepared using the procedure described for the synthesis of 5-butyl-2-(N-t-butylaminosulfonyl)-thiophene by substituting isobutyliodide for butyliodide. Rf=0.37 (6:1 Hex/EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05444067 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-93aa92d9526d484cb2a5aece2235cd0c |
| Source note | uspto-grants-1995_08 |