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HRID 225410作成日:2026年10月27日

1,2,6-Hexanetriol → 1,3-Dioxolane-4-butanol, 2-phenyl-

https://huagongshe.com/reaction/225410

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,6-HexanetriolHCID 7823—
反応物Benzaldehyde dimethyl acetalHCID 62375—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1,3-Dioxolane-4-butanol, 2-phenyl-HCID 23668066.3%

反応条件

温度100 °C

反応手順

To a solution of 1,2,6-trihydroxyhexane (10.0 g, 74.6 mmol) and benzaldehyde dimethylacetal (15.0 g, 98.7 mmol) in dry DMF (10 mL) was added Amberlyst 15 (5.0 g). The mixture was stirred at 100° C. for 5 min, then cooled and filtered. The filtrate was concentrated and residue obtained was re-dissolved in ethyl acetate. After being washed with water and brine, the solution was dried over Na2SO4. The crude product obtained after evaporation of the solvent was chromatographed on silica eluting with ethyl acetate. Concentration of the proper fractions afforded 11.0 g (66%) of the title product (a mixture of diastereomers) as a colorless oil: 1H NMR (CDCl3, 300 MHz, ppm) 7.48 (m, 2H), 7.39 (m, 3H), 5.92 (s, 0.4H), 5.80 (s, 0.6H), 4.3-4.1 (m, 2H), 3.64 (m, 3H), 1.8-1.4 (m, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07556923B1
出典データセットuspto-grants-2009_07
ORD IDord-890a35a252d748c185edeceb8dcd8ed1
出典メモuspto-grants-2009_07