HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl morpholine oxide → 6-chloro-N-(2,3-dihydroxypropyl)-N-phenylpyridine-3-sulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl morpholine oxide | HCID 82029 | — |
| Edukt | Tetrahydrofuran hexane | HCID 21883165 | — |
| Edukt | 6-chloro-N-phenyl-N-(prop-2-en-1-yl)pyridine-3-sulfonamide | HCID 24419482 | — |
| Katalysator | Osmium Tetroxide | HCID 30318 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 6-chloro-N-(2,3-dihydroxypropyl)-N-phenylpyridine-3-sulfonamide | HCID 86659756 | 80% |
Reaktionsschritte
To a solution of 1.3 g (4.2 mmol) of 6-chloro-N-phenyl-N-(prop-2-en-1-yl)pyridine-3-sulfonamide in 17 mL of a mixture (1/1) of tBuOH and water are added, at room temperature, 1.37 g (11.7 mmol) of NMO and 0.52 mL (0.04 mmol) of 2.5% OsO4 in tBuOH. Stirring is continued for 12 hours. The medium is then diluted with 200 mL of water and extracted with Et2O (2×100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. 1.14 g of 6-chloro-N-(2,3-dihydroxypropyl)-N-phenylpyridine-3-sulfonamide are obtained in the form of an oil, which is used without further purification in the following step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08541455B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-4e96f7796f8746948ad806fa4b810484 |
| Quellennotiz | uspto-grants-2013_09 |