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HRID 1654776作成日:2026年10月26日

Benzaldehyde → alpha-[(2-Furanyl)ethynyl]-benzenemethanol

https://huagongshe.com/reaction/1654776

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Furan, 2-ethynyl-HCID 140409—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-[(2-Furanyl)ethynyl]-benzenemethanolHCID 20076917—

反応手順

Place lithium hexamethyldisilazane (3 mL of a 1M solution in tetrahydrofuran, 3 mmol) under argon atmosphere and cool to 0° C. Add 2-furanylacetylene (276 mg, 3 mmol) in tetrahydrofuran (20 mL) and stir at 0° C. until anion formation is complete. Add a solution of benzaldehyde (297 mg, 2.8 mmol) in tetrahydrofuran, remove the ice bath and stir at room temperature until the reaction is complete. Pour onto ethyl ether and water, separate the organic layer and dry (MgSO4). Filter and evaporate the solvent in vacuo. Purify by silica gel chromatography to yield the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05409942
出典データセットuspto-grants-1995_04
ORD IDord-2e9f376ed6604e7fa0f13a36388ca523
出典メモuspto-grants-1995_04