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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857814Generated: October 26, 2026

Nitrogen → Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonate

https://huagongshe.com/reaction/857814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
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 N2. 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07147936B2
Source datasetuspto-grants-2006_12
ORD IDord-8da8d49b223949588fe7763258526ffb
Source noteuspto-grants-2006_12