戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 271191作成日:2026年10月25日

Diisobutylaluminumhydride → [3,5-Dibromo-4-(bromomethyl)phenyl]methanol

https://huagongshe.com/reaction/271191

反応式

関与物質

役割名称HCID仕込み量
反応物DiisobutylaluminumhydrideHCID 21225700—
反応物Methyl 3,5-dibromo-4-(bromomethyl)benzoateHCID 22647948—
溶媒TetrahydrofuranHCID 8028—
生成物[3,5-Dibromo-4-(bromomethyl)phenyl]methanolHCID 5983448794.5%

反応条件

温度0 °C

反応手順

A solution of 3,5-dibromo-4-bromomethyl-benzoic acid methyl ester (57) (5.2 g, 13.44 mmol) in tetrahydrofuran (50 mL) at 0° C. was treated with a 1M solution of diisobutylaluminum hydride in tetrahydrofuran (30 mL, 30 mmol). The reaction mixture was stirred for 2 h at 0° C. TLC revealed starting material was still present. Additional 1M solution of diisobutylaluminum hydride in tetrahydrofuran (16 mL, 16 mmol) was added at 0° C. and the reaction mixture was stirred for 30 min at 0° C. The reaction was quenched cautiously by pouring it onto a mixture of ice and concentrated hydrochloric acid (100 mL) and the mixture was extracted with ethyl acetate (3×150 mL). The organic layers were combined, dried with magnesium sulfate, filtered, and concentrated under vacuum to afford a solid which was dried under high vacuum to afford (3,5-dibromo-4-bromomethyl-phenyl)-methanol (58) (4.56 g, 94%) as an off-white solid; LRMS-EI(+) for C8H7Br3O (M+) m/z=356. MW=358.8564, Exact Mass=355.8047

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452882B2
出典データセットuspto-grants-2008_11
ORD IDord-cc80a4d6f3c047f89b5385f85d376c6e
出典メモuspto-grants-2008_11