HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrogen Bromide → (2S,3R,4S,5S)-2-bromotetrahydro-2H-thiopyran-3,4,5-triyl triacetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose | HCID 10991244 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | 1,1-Dichloroethane | HCID 6365 | — |
| Produkt | (2S,3R,4S,5S)-2-bromotetrahydro-2H-thiopyran-3,4,5-triyl triacetate | HCID 10948230 | 39% |
Reaktionsschritte
3.50 ml of a 30% solution of hydrobromic acid in glacial acetic acid are added at 10° C. to a solution of 2.10 g (6.3.10-3 mol) of 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose in 10 cm3 of dichloroethane. After 2 to 3 h, the reaction medium is hydrolyzed, washed with a solution of sodium bicarbonate and dried over sodium sulfate (Na2SO4) and the solvent is evaporated off to dryness under reduced pressure. 0.87 g (yield: 39%) of the expected product is obtained after precipitation in ether.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05246961 |
| Quelldatensatz | uspto-grants-1993_09 |
| ORD ID | ord-826a99c45042499d9978bfa9b6772ca8 |
| Quellennotiz | uspto-grants-1993_09 |