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HRID 42750作成日:2026年10月25日

Ethylene Glycol → 2-(4-Bromobutyl)-2-methyl-1,3-dioxolane

https://huagongshe.com/reaction/42750

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NitrogenHCID 947—
反応物p-Toluenesulfonic acidHCID 6101—
反応物6-Bromohexan-2-oneHCID 25061—
反応物Sodium BicarbonateHCID 516892—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物2-(4-Bromobutyl)-2-methyl-1,3-dioxolaneHCID 560013—

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and a Dean-Stark under inert atmosphere (N2), a solution of 6-bromo-hexan-2-one (3.34 g, 18.65 mmol) in toluene (71.3 mL) was treated with ethylene glycol (10.4 mL, 186.92 mmol) and TsOH (35 mg, 0.19 mmol). The reaction mixture was heated to reflux for 3 h, allowed to cool to rt and sat. aq. NaHCO3 (100 mL) and ether (100 mL) were added and the aq. phase was washed with water (2×100 mL), dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound. 1H NMR (400 MHz, CDCl3) δ1.34 (s, 3H), 1.50-1.65 (m, 2H), 1.65-1.75 (m, 2H), 1.84-1.98 (m, 2H), 3.43 (t, J=6.8 Hz, 2H), 3.90-4.04 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536209B2
出典データセットuspto-grants-2013_09
ORD IDord-1f37e5b7d2814e2bb7eb2867e6bdecb9
出典メモuspto-grants-2013_09