HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → Acetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Edukt | 3-Butene-1,2-diol | HCID 10338 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | Acetate | HCID 175 | — |
| Produkt | p-Toluenesulfonate | HCID 85570 | — |
Reaktionsschritte
The racemic acetate substrate was prepared by one of two methods. The diol route began with racemic 1,2-dihydroxy-3-butene which could be prepared by reacting EpB with water under neutral conditions or with acid catalysis. The diol was treated with p-toluenesulfonyl chloride (p-TsCl) in pyridine at 4° C. to afford the desired monotosylate contaminated with about 10% of the corresponding ditosylate. The monotosylate could be selectively crystallized to afford pure monotosylate in 61% yield. Hydroxytosylate was acetylated under normal conditions (Ac2O, Et3N, CH2Cl2) to provide the acetoxy-tosylate (the desired racemic acetate) in 93% yield. The diol route is illustrated as follows: ##STR3##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05126268 |
| Quelldatensatz | uspto-grants-1992_06 |
| ORD ID | ord-43103bb205504cc5b58c81ebba3f1cb6 |
| Quellennotiz | uspto-grants-1992_06 |