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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825692Generated: October 26, 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/reaction/1825692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Butane sultoneHCID 15411—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dihydrothieno(3,4-b)-1,4-dioxin-2-methanolHCID 16067438—
SolventTetrahydrofuranHCID 8028—
ProductSodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonateHCID 23588691—

Reaction Conditions

Temperature25 °C

Reaction Steps

(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. Sodium hydride (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 hexanes 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-sulfonic acid sodium salt as was demonstrated by NMR and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07048874B2
Source datasetuspto-grants-2006_05
ORD IDord-b69d140b944a43d4b44f3e9b33fc5b6b
Source noteuspto-grants-2006_05