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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23756생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/23756

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물1,2,6-HexanetriolHCID 7823—
반응물3,4-Di-n-propoxythiopheneHCID 11401397—
생성물4-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanolHCID 22590342—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852831B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-d92287d6b2ae41aa84fbe9104e260357
출처 메모uspto-grants-2005_02