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HRID 30469作成日:2026年10月24日

(5-Bromo-3-pyridinyl)methanol → 5-Bromo-3-pyridinecarboxaldehyde

https://huagongshe.com/ja/reaction/30469

反応式

関与物質

役割名称HCID仕込み量
反応物(5-Bromo-3-pyridinyl)methanolHCID 2784733—
触媒Manganese dioxideHCID 14801—
生成物5-Bromo-3-pyridinecarboxaldehydeHCID 278473451.1%

反応手順

(5-Bromo-pyridin-3-yl)-methanol (1.13 g, 6.00 mmol) was dissolved in CHCI3 (40 mL) and treated with MnO2 (3.60 g). The reaction mixture was heated at reflux temperature for 3 h. The hot reaction mixture was filtered through a pad of diatomaceous earth and the filtrate was concentrated to yield the title compound (0.570 g, 51%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423147B2
出典データセットuspto-grants-2008_09
ORD IDord-a363896c2f4243088d27486a0d5c3e7a
出典メモuspto-grants-2008_09