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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 1,4-Butane sultone | HCID 15411 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Dihydrothieno(3,4-b)-1,4-dioxin-2-methanol | HCID 16067438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonate | HCID 23588691 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07147936B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-8da8d49b223949588fe7763258526ffb |
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| Source note | uspto-grants-2006_12 |
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