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HRID 9814作成日:2026年10月24日

Triphenylphosphine → 1-Bromooct-3-yne

https://huagongshe.com/ja/reaction/9814

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物N-bromobutanimideHCID 67184—
反応物3-Octyn-1-olHCID 84694—
溶媒DimethylformamideHCID 6228—
生成物1-Bromooct-3-yneHCID 1247620671.4%

反応条件

温度0 °C

反応手順

To a solution of oct-3-yn-1-ol (1.26 g, 10.0 mmol) in DMF (25 mL) was added triphenylphosphine (2.92 g, 11.2 mmol). The solution was cooled to 0° C. and NBS (1.92 g, 10.8 mmol) was added in portions. After stirring for 30 min at room temperature, the reaction was quenched with methanol (1 mL). The solution was diluted with ether (150 mL), washed with water, saturated aqueous NaHCO3 and brine successively. The organic layer was dried and concentrated. The residue was purified by flash chromatography on silica gel, eluting with hexane to afford 1-bromo-oct-3-yne (1.35 g, 71%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 3.40 (2H, d, J=7.2 Hz), 2.78 (2H, m), 2.15 (2H, m), 1.22 (4H, m), 0.88 (3H, t, J=6.9 Hz); 13C NMR (75 MHz, CDCl3) δ 82.83, 77.05, 31.18, 30.63, 23.68, 22.20, 18.67, 13.89.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091357B2
出典データセットuspto-grants-2006_08
ORD IDord-d45dd811ad1242be89b10cf1539f2c95
出典メモuspto-grants-2006_08