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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827637Generated: 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/1827637

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. 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 5 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056600B2
Source datasetuspto-grants-2006_06
ORD IDord-cd186954ca404a55bd09c2108542bbe0
Source noteuspto-grants-2006_06