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HRID 9795作成日:2026年10月23日

Triphenylphosphine → 10-Bromo-1-decene

https://huagongshe.com/ja/reaction/9795

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物9-Decen-1-olHCID 25612—
反応物N-bromobutanimideHCID 67184—
溶媒DimethylformamideHCID 6228—
生成物10-Bromo-1-deceneHCID 54338481%

反応条件

温度0 °C

反応手順

To a solution of dec-9-en-1-ol (1.22 g, 7.82 mmol) in DMF (18 mL) was added triphenylphosphine (2.30 g, 8.77 mmol). The solution was cooled to 0° C. and NBS (1.52 g, 8.54 mmol) was added in portions. After stirring for 30 min at room temperature, the reaction was quenched with methanol (0.8 mL). The solution was diluted with ether (80 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 10-bromo-dec-1-ene (1.38 g, 81%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.80 (1H, m), 4.94 (2H, m), 3.38 (2H, t, J=6.9 Hz), 2.02 (2H, m), 1.83 (2H, m), 1.20–1.55 (10H, m); 13C NMR (75 MHz, CDCl3) δ 139.17, 114.30, 34.29, 34.02, 33.06, 29.53, 29.25, 29.12, 28.96, 28.40.

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-1e3ad5c77d6a4913a7de709d2d308fb0
出典メモuspto-grants-2006_08