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HRID 1816596作成日:2026年10月25日

Hydrochloric Acid → (5-Bromo-2,3-dimethoxyphenyl)methanol

https://huagongshe.com/reaction/1816596

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物5-Bromo-2,3-dimethoxybenzaldehydeHCID 322405—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Bromo-2,3-dimethoxyphenyl)methanolHCID 219409095.5%

反応手順

10.67 g of 5-bromo-2,3-dimethoxybenzaldehyde was dissolved in 100 ml tetrahydrofuran and 100 ml ethanol. 1 g of sodium borohydride was added thereto, followed by stirring overnight at room temperature. After adding 1 N hydrochloric acid thereto, the reaction solution was extracted with ethyl acetate, and the organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated, to give 10.27 g of 5-bromo-2,3-dimethoxybenzyl alcohol. 5.326 g of this crude product was dissolved in 50 ml N,N-dimethylformamide, and 1.8 g of imidazole and 5.9 g of tertiary butyl chlorodiphenyl silane were added, and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was evpoarated, to give 10.72 g of [(5-bromo-2,3-dimethoxybenzyl)oxy](tertiary butyl)diphenylsilane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06884821B1
出典データセットuspto-grants-2005_04
ORD IDord-2a715fa163dd400bbad657b9fe6ea544
出典メモuspto-grants-2005_04