HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 489589Erstellt: 24. Oktober 2026
1,4-Butane sultone → Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonate
https://huagongshe.com/de/reaction/489589
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,4-Butane sultone | HCID 15411 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2,3-Dihydrothieno(3,4-b)-1,4-dioxin-2-methanol | HCID 16067438 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonate | HCID 23588691 | — |
Reaktionsschritte
(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol (6.9 g, 40 mmol) was dissolved into tetrahydrofuran (100 mL) and blanketed by nitrogen. NaH (1.76 g) was added and stirring was continued for 30 min. Then butanesultone (6.0 g) was added dropwise after which the reaction mixture was brought to reflux for 3 h. Then it was cooled to 25° C. again, the solvent was removed, methanol was added, the mixture was stirred, filtered and the filtrate was concentrated. The remaining oil was solidified by addition of hexane and ethanol, followed by stirring. Final filtration and drying resulted in pure 4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-butane-1-sulphonic acid sodium salt as was demonstrated by NMR and mass spectroscopy.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06977390B2 |
|---|
| Quelldatensatz | uspto-grants-2005_12 |
|---|
| ORD ID | ord-690c6949eee1492aba64887b417a4129 |
|---|
| Quellennotiz | uspto-grants-2005_12 |
|---|