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HRID 1910647作成日:2026年10月25日

Diethyl Ether → 1-(5-Chloro-2,3-dimethoxyphenyl)ethanol

https://huagongshe.com/reaction/1910647

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Ammonium ChlorideHCID 25517—
反応物5-Chloro-2,3-dimethoxybenzaldehydeHCID 4172275—
反応物HCID 178418573HCID 178418573—
溶媒tert-Butyl methyl etherHCID 15413—
生成物1-(5-Chloro-2,3-dimethoxyphenyl)ethanolHCID 1409291596%

反応条件

温度33 °C

反応手順

To a mixture of 5-chloro-2,3-dimethoxybenzaldehyde (339, 1.69 mol) in TBME (5.6 L) was added 3M methylmagnesium bromide in ether (660 mL, 1.98 mol) over 1 hour at 9 to 12° C. The mixture was warmed at 33° C. for 1 hour 20 minutes. There was significant starting material present so more methylmagnesium bromide was added (590 mL, 1.77 mol) over 1 hour 20 minutes with the reaction temperature at 33° C. The reaction was cooled to room temperature overnight and poured into ammonium chloride (20 wt %, 3 kg) over 5 minutes. The temperature rose from 11 to 28° C. The reaction flask was rinsed with ammonium chloride solution (500 mL) and TBME (250 mL). The layers were separated and the organic layer was concentrated to an orange yellow thick oil. Yield: 348 g (96% yield, 94% purity).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08604021B2
出典データセットuspto-grants-2013_12
ORD IDord-f6e6fe890c894580bd2710ff3326b314
出典メモuspto-grants-2013_12