戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1294527作成日:2026年10月27日

Triphenylphosphine → Phosphonium, [3-(methoxymethoxy)propyl]triphenyl-, bromide

https://huagongshe.com/reaction/1294527

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物1-Bromo-3-methoxymethoxypropaneHCID 12709288—
溶媒TolueneHCID 1140—
生成物Phosphonium, [3-(methoxymethoxy)propyl]triphenyl-, bromideHCID 11178287—

反応条件

温度100 °C

反応手順

To a solution of 1-bromo-3-(methoxymethoxy)propane (0.46 g, 2.5 mmol) in anhydrous toluene (1.5 mL) was added triphenylphoshine (0.71 g, 2.7 mmol) under argon with stirring. The mixture was heated at 100° C. for 20 h and cooled to room temperature. The liquid was decanted and the solid residue was grounded with spatula, filtered and washed several times with ether. After drying overnight in vacuum dessicator colorless crystals of phosphonium salt A (0.98 g, 88%) could be used in the Wittig reaction without further purification. A: 1H NMR (500 MHz, CDCl3) δ 1.96 (2H, m, CH2—CH2—CH2), 3.31 (3H, s, O—CH3), 3.85 (2H, br t, J=5.6 Hz, CH2—CH2—O), 4.00 (2H, m, P—CH2), 4.60 (2H, s, O—CH2—O), 7.70, 7.79 and 7.86 (6H, 3H and 6H, each m, Ar—H); Anal. Calcd for C23H26O2PBr: C, 62.03, H, 5.88, Br, 17.94. Found: C, 61.87, H, 5.77, Br, 17.89.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07241747B2
出典データセットuspto-grants-2007_07
ORD IDord-56d7602860a646f381294e81d49a2428
出典メモuspto-grants-2007_07