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HRID 41248作成日:2026年10月25日

Tetrahydrofuran → 1-(4-Bromo-3,5-dimethoxyphenyl)ethanol

https://huagongshe.com/reaction/41248

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Ammonium ChlorideHCID 25517—
反応物(4-Bromo-3,5-dimethoxyphenyl)methanolHCID 11149289—
反応物HCID 178418348HCID 178418348—
触媒HCID 178418406HCID 178418406—
溶媒TolueneHCID 1140—
溶媒1,1-DichloroethaneHCID 6365—
生成物1-(4-Bromo-3,5-dimethoxyphenyl)ethanolHCID 58223484—

反応条件

温度80 °C

反応手順

To a solution of (4-bromo-3,5-dimethoxyphenyl)methanol (14.5 g, 58.7 mmol) in dichloroethane (100 ml) and toluene (140 mL) was added manganese dioxide (25.5 g, 294 mmol) and the mixture was stirred at 80° C. for three hours. After the reaction was completed, the mixture was filtered with Celite and the solvent was distilled off under reduced pressure to obtain a crude compound. To a tetrahydrofuran (153 mL) solution of the crude compound (13.8 g, 56.3 mmol) was added dropwise 1.04M methyllithium (59.5 mL, 61.9 mmol) at −78° C., and the mixture was stirred for four hours. After the reaction was completed, a saturated aqueous solution of ammonium chloride was added to the reaction mixture, which was extracted with ethyl acetate, and dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-heptane/ethyl acetate: 4/1 then 1/1) to obtain the title compound (11.4 g, 43.7 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530504B2
出典データセットuspto-grants-2013_09
ORD IDord-5d0b48b62aa342f7a83e6131f901f3df
出典メモuspto-grants-2013_09