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HRID 659139作成日:2026年10月27日

Benzaldehyde → alpha-Ethynylbenzenemethanol

https://huagongshe.com/reaction/659139

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178418486HCID 178418486—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-EthynylbenzenemethanolHCID 20155—

反応手順

To a solution of 2.65 g of benzaldehyde (Formula 26) in 50 mL of THF at room temperature was added 100 mL of 0.5M ethynylmagnesium bromide in THF. The mixture was stirred at room temperature for 2 hours. Then, the mixture was diluted with diethylether and a saturated solution of ammonium chloride. The mixture was extracted with ethyl acetate. Combined ethyl acetate was washed with brine, dried over sodium sulfate and concentrated. Column chromatography (20% ethyl acetate/hexane) gave 3.17 g of 1-phenyl-prop-2-yn-1-ol (Formula 27) as a light yellow oil. 1H NMR (300 MHz, CDCl3) δ 2.68 (m, 1H), 5.46-5.49 (m, 1H), 7.34-7.43 (m, 3H), 7.55-7.57 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08080570B2
出典データセットuspto-grants-2011_12
ORD IDord-54eda138bf08464bbbf77e5d0f0fbb67
出典メモuspto-grants-2011_12