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HRID 489589作成日:2026年10月26日

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/489589

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Butane sultoneHCID 15411—
反応物Sodium hydrideHCID 24758—
反応物2,3-Dihydrothieno(3,4-b)-1,4-dioxin-2-methanolHCID 16067438—
溶媒TetrahydrofuranHCID 8028—
生成物Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonateHCID 23588691—

反応条件

温度25 °C

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06977390B2
出典データセットuspto-grants-2005_12
ORD IDord-690c6949eee1492aba64887b417a4129
出典メモuspto-grants-2005_12