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HRID 52392作成日:2026年10月25日

Propargyl bromide → 2-Propargyloxy-2-phenyl-3-butyne

https://huagongshe.com/reaction/52392

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl bromideHCID 7842—
反応物Sodium HydroxideHCID 14798—
反応物3-Hydroxy-3-phenyl-1-butyneHCID 92098—
反応物Tetrabutyl ammonium hydrogen sulfate waterHCID 86750630—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
生成物2-Propargyloxy-2-phenyl-3-butyneHCID 1125239265%

反応手順

Propargyl bromide (22 g, 0.15 mol) was dissolved in 140 ml of n-hexane. This solution, 2-phenyl-3-butyne-2-ol (14.6 g, 0.1 mol), NaOH (60 g, 1.5 mol) and a catalytic amount of tetrabutyl ammonium hydrogen sulfate/water (120 ml) were mixed, reacted for 24 hours at an ambient temperature and refluxed for 30 minutes. After completion of the reaction, the mixture was cooled to an ambient temperature and water (100 ml) was added. The organic phase was extracted with 30 ml of n-hexane, three times. The extracted organic solvent was dried with anhydrous magnesium sulfate, filtered and evaporated to separate. b.p.: 61° C./0.5 mmHg; yield: 65%; MS: m/e 184 (parent), 129 (base).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616669
出典データセットuspto-grants-1997_04
ORD IDord-0eda761b3ecf455a8a5934f3ae9aab88
出典メモuspto-grants-1997_04