戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2361166作成日:2026年10月26日

Ethyl orthoformate → 3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenol

https://huagongshe.com/reaction/2361166

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl orthoformateHCID 31214—
反応物Neopentyl glycolHCID 31344—
反応物6-Bromo-2-hydroxy-3-methoxybenzaldehydeHCID 262237—
触媒p-Toluenesulfonic acidHCID 6101—
生成物3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenolHCID 59761836100%

反応条件

温度110 °C

反応手順

A mixture of 6-bromo-2-hydroxy-3-methoxy-benzaldehyde (2.31 g, 10.0 mmol), neopentyl glycol (1.14 g, 11.0 mmol), TsOH (9.5 mg) and triethyl orthoformate (1.93 g, 13.0 mmol) were heated at 110° C. for 30 min and then partitioned between NaHCO3 (300 mL) solution and EtOAc (200 mL). The aqueous layer was extracted with EtOAc (3×30 mL) and the combined extracts were washed with brine and dried through Na2SO4. Evaporation of solvent afforded the title compound (3.17 g, 100%). 1H NMR (CDCl3) δ 0.85 (s, 3H), 1.27 (s, 3H), 3.70 (s, 2H), 3.82 (s, 2H), 3.85 (s, 3H), 5.90 (s, 1H), 6.72 (d, J=8 Hz, 1H), 7.02 (d, J=8 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08686005B2
出典データセットuspto-grants-2014_04
ORD IDord-13e61ff272674b1bbad8583fee98da4d
出典メモuspto-grants-2014_04