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HRID 23756作成日:2026年10月25日

p-Toluenesulfonic acid → 4-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol

https://huagongshe.com/reaction/23756

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物1,2,6-HexanetriolHCID 7823—
反応物3,4-Di-n-propoxythiopheneHCID 11401397—
生成物4-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanolHCID 22590342—

反応手順

9.06 g (45.2 mmol) of 3,4-di-n-propoxythiophene, 30.3 g (226 mmol) of 1,2,6-hexanetriol and 0.09 g (0.5 mmol) of p-toluenesulphonic acid are heated to 150 to 165° C. (bath temperature) under N2 for 3 h. During this time, 5.8 g of distillate (substantially n-propanol) were collected. The cooled liquid was diluted with 50 ml of methylene chloride, washed to neutrality and to free it of hexanetriol with water and the organic phase was dried over Na2SO4. After filtering and evaporating the methylene chloride, the residue (6.73 g=74.8% of theory) was identified by 1H NMR spectroscopy (in CDCl3 against TMS) using δ=6.30 ppm (2H, thiophene H) and 2.85 ppm (1H, OH) as being substantially 4-(2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852831B2
出典データセットuspto-grants-2005_02
ORD IDord-d92287d6b2ae41aa84fbe9104e260357
出典メモuspto-grants-2005_02