戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 250522作成日:2026年10月26日

Ethylene Glycol → 2-Methyl-2-(4-methylphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/250522

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物p-Toluenesulfonic acidHCID 6101—
反応物p-METHYLACETOPHENONEHCID 8500—
溶媒TolueneHCID 1140—
生成物2-Methyl-2-(4-methylphenyl)-1,3-dioxolaneHCID 275546979.1%

反応手順

A mixture of 4-methylacetophenone (1.00 g, 7.45 mmol), p-toluenesulfonic acid (133 mg, 0.745 mmol) and ethylene glycol (1.20 mL, 22.4 mmol) in dry toluene (20 mL) was heated at reflux with a Dean-Stark apparatus under nitrogen for 24 h. The mixture was allowed to cool to room temperature and the solvent was evaporated in vacuo. The residue was taken up in ether (20 mL) and the solution was washed with saturated sodium bicarbonate solution (2×10 mL) and brine (1×10 mL), then dried (Na2SO4) and concentrated under reduced pressure. Flash column chromatography of the residue, eluting with 37% aqueous ammonia:ether:hexane (0.02:1:6) afforded 2-methyl-2-(4-methylphenyl)-1,3-dioxolane (23) as a colourless oil (1.05 g, 59%). 1H nmr (200 MHz, CDCl3) 1.65 (s, 3H, CH3), 2.35 (s, 3H, ArCH3), 3.74-3.86 (m, 2H, OCH2), 3.94-4.06 (m, 2H, OCH2), 7.15 (d, J=8.2 Hz, 2H, 2×ArH), 7.37 (d, J=8.2 Hz, 2H, 2×ArH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863313B2
出典データセットuspto-grants-2011_01
ORD IDord-125d60b86bf04bc18b8c7532c6023856
出典メモuspto-grants-2011_01