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HRID 64243作成日:2026年10月25日

Triphenylphosphine → (But-3-yn-2-yloxy) Benzene

https://huagongshe.com/reaction/64243

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-Butyn-2-olHCID 16239—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物1-(3-(1-Hydroxy-1-methylethyl)phenyl)ethanoneHCID 13531419—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(But-3-yn-2-yloxy) BenzeneHCID 12519596—

反応手順

Phenol 27 (422.9 mg, 4.49 mmol), But-3-yn-2-ol (300 mg, 4.28 mmol) were dissolved in anhydrous THF (10 mL) under N2 atmosphere, at 0° C. was added Ph3P (1.12 g, 4.26 mmol) portion wise, stirred it for 10 min, and then DEAD (894.6 mg, 5.14 mmol) added slowly. The resultant solution was heated up to 70° C. stirred for 20 h. To the reaction mixture water added and extracted with DCM and dried organic layer on MgSO4, filtered, concentrated. Purified by flash chromatography using ethylacetate/n-hexane, 5:95) provided compound 28 (450 mg, 69%) as a solid. 1H NMR (CDCl3, 400 MHz) δ 1.67 (d, J=6.8 Hz, 3H), 2.47 (d, J=2 Hz, 1H), 4.88 (q, J=2 Hz, 1H), 6.97-7.03 (m, 3H), 7.28-7.32 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447134B2
出典データセットuspto-grants-2016_09
ORD IDord-c87323b5de76448da663a06fe061e6df
出典メモuspto-grants-2016_09