HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → 5-Ethynylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 5-Bromo-2-thiophenesulfonamide | HCID 1241304 | — |
| Product | 5-Ethynylthiophene-2-sulfonamide | HCID 86043795 | — |
Reaction Steps
Prepared from 5-bromo-thiophene-2-sulfonic acid amide (1.94 g, 8 mmol) and trimethylsilylacetylene (2.2 mL, 12 mmol) by applying in analogous manner the procedures described in example D.1 (method 1, steps 1–2). Obtained after chromatographic purification of the crude product (SiO2, 0–75% AcOEt/heptane) as a light brown solid (0.49 g, 33%). MS (ISP) 186.1 [(M−H)−]; mp 114–116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238808B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-1f6620eaf5fb4cec9290219b90a1ae39 |
| Source note | uspto-grants-2007_07 |