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HRID 30611作成日:2026年10月25日

p-Toluenesulfonic acid → 3-[1,3]Dioxan-2-yl-2'-methyl-biphenyl-4-ol

https://huagongshe.com/reaction/30611

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1,3-PropanediolHCID 10442—
反応物4-Hydroxy-2'-methyl[1,1'-biphenyl]-3-carbaldehydeHCID 20099867—
溶媒TolueneHCID 1140—
生成物3-[1,3]Dioxan-2-yl-2'-methyl-biphenyl-4-olHCID 6921762989%

反応手順

A solution of 4-hydroxy-2′-methyl-biphenyl-3-carbaldehyde (18.8 mmol) in toluene (100 mL) was added 1,3-dihydroxypropane (65.7 mmol) and p-toluenesulfonic acid (cat) and heated at reflux overnight in a Dean-Stark set-up. The reaction was cooled and washed with a solution of Na2CO3 (aq, 1 M). Evaporation in vacuo gave the title product as brown oil in 89% yield. 1H-NMR (CDCl3) δ 9.61 (bs, 1H), 7.34-7.10 (m, 6H), 6.87 (d, 1H), 5.77 (s,1H), 4.13-4.07 (m, 2H), 3.95-3.86 (m, 2H), 2.20 (s, 3H), 2.18-1.96 (m, 1H), 1.40 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423181B2
出典データセットuspto-grants-2008_09
ORD IDord-12868647474649d7a47cf0fd64862070
出典メモuspto-grants-2008_09