HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 5-Bromopyridine-3-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Bromopyridine-3-sulphonic acid | HCID 12684261 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 5-Bromopyridine-3-sulfonyl chloride | HCID 20324474 | 98.4% |
Reaction Steps
A mixture of 5-bromo-pyridine-3-sulfonic acid (Example B.2 step 1) (7.14 g, 30 mmol), phosphorus pentachloride (9.68 g, 47 mmol) and phosphorus oxychloride (20 mL) was heated to reflux for 4 h (according to J. Org. Chem. 1989, 54(2), 389). The reaction mixture was concentrated to dryness to give a yellow semisolid, dissolved in ice water and tert-butyl-methyl-ether, and cautiously added sat. NaHCO3-sol. until neutralized, saturated with solid NaCl, separated phases, dried organic layer over Na2SO4. Removal of the solvent in vacuum gave the title compound as a yellow solid (7.57 g, 98%). MS (EI) 254.9 [(M)+], 256.9 [(M+2)+] and 258.9 [(M+4)+]; mp 64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063048B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-b8facc8fe3b04f4fae5f28b0cb01461a |
| Source note | uspto-grants-2011_11 |