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HRID 9823作成日:2026年10月24日

Triphenylphosphine → 1-Bromo-7-methyloctane

https://huagongshe.com/ja/reaction/9823

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物IsononanolHCID 17072—
反応物N-bromobutanimideHCID 67184—
溶媒DimethylformamideHCID 6228—
生成物1-Bromo-7-methyloctaneHCID 1363478174.2%

反応条件

温度0 °C

反応手順

To a solution of 7-methyl-octan-1-ol (1.20 g, 8.33 mmol) in DMF (20 mL) was added triphenylphosphine (2.43 g, 9.26 mmol). The solution was cooled to 0° C. and NBS (1.60 g, 8.99 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 (100 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-7-methyl-octane (1.28 g, 74%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 3.41 (2H, t, J=6.6 Hz), 1.85 (2H, m), 1.52 (1H, m), 1.42 (2H, m), 1.28 (4H, m), 1.17 (2H, m), 0.87 (3H, s), 0.85 (3H, s); 13C NMR (75 MHz, CDCl3) δ 39.16, 34.34, 33.14, 29.34, 28.52, 28.24, 27.51, 22.94.

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-1dcf53a9a79d4a13b5884fe5d9b1212b
出典メモuspto-grants-2006_08