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HRID 496809作成日:2026年10月25日

Water → 2-Bromo-3-cyclohexyloxy pyridine

https://huagongshe.com/reaction/496809

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cyclohexyl bromideHCID 7960—
反応物2-Bromo-3-pyridinolHCID 23070—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
生成物2-Bromo-3-cyclohexyloxy pyridineHCID 2232336030%

反応手順

Sodium hydride (160 mg) was dissolved in dimethylformamide (5 ml) and 2-bromo-3-pyridinol (500 mg) dissolved in dimethylformamide is slowly added dropwise. Then, bromocyclohexane (0.7 ml) was added to the solution and reacted for 5 hours at room temperature. Water was added to the suspension to dilute and extracted with ethyl acetate to separate an organic layer. The separated organic layer was dried with anhydrous magnesium sulfate and distilled under reduced pressure. As a result, 2-bromo-3-cyclohexyloxy pyridine (220 mg, yield: 30%) was obtained as an oil phase.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06946558B2
出典データセットuspto-grants-2005_09
ORD IDord-048d469ce30545f59c35fb3fe46cfc7d
出典メモuspto-grants-2005_09