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HRID 45474作成日:2026年10月23日

Ammonium Chloride → 1-(2'-(Benzyloxy)-3'-tert-butylbiphenyl-3-yl)-1-(2-methoxyphenyl)ethanol

https://huagongshe.com/ja/reaction/45474

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1-(2'-(Benzyloxy)-3'-tert-butylbiphenyl-3-yl)ethanoneHCID 58238598—
反応物HCID 178489560HCID 178489560—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2'-(Benzyloxy)-3'-tert-butylbiphenyl-3-yl)-1-(2-methoxyphenyl)ethanolHCID 58238599—

反応手順

A solution of 36 (0.8 g, 2.23 mmol) in anhydrous tetrahydrofuran (8 mL) was stirred under nitrogen at room temperature and 1M ortho-methoxyphenyl magnesium bromide in tetrahydrofuran (3 mL, 1.35 equiv.) was slowly added. Stirring was continued at room temperature for 30 min and at 60° C. for 3 hr. After cooling, the reaction mixture was poured on saturated ammonium chloride (120 mL) and extracted with ethyl acetate (150 mL). The organic extract was washed with water (2×50 mL), dried over sodium sulfate and filtered. The solvent was removed in a rotary evaporator and the crude 37 thus obtained was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541522B2
出典データセットuspto-grants-2013_09
ORD IDord-d0dbe5b4edf345aa848c9fad3f26678e
出典メモuspto-grants-2013_09