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HRID 366309作成日:2026年10月26日

Bis(2-ethylhexyl)amine → 3,3,3-Trifluoropropyl bis(2-ethylhexyl)aminodimethoxysilane

https://huagongshe.com/reaction/366309

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-ethylhexyl)amineHCID 7791—
反応物3,3,3-Trifluoropropyl-trimethoxysilaneHCID 67933—
反応物Bis(2-ethylhexyl)aminodimethoxysilaneHCID 131722118—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物3,3,3-Trifluoropropyl bis(2-ethylhexyl)aminodimethoxysilaneHCID 2328914798%

反応条件

温度15 °C

反応手順

3,3,3-Trifluoropropyl(bis(2-ethylhexyl)aminodimethoxysilane--A 500 mL round bottomed flask was charged with tetrahydrofuran (300 mL) and isopropylmagnesium chloride (25 mL of a 2.0 M solution in THF, 50 mmol). The contents were cooled to 15° C. Bis(2-ethylhexyl)amine (50 mmol) was added over fifteen minutes via pressure equalizing addition funnel. The cold bath was removed and the contents stirred for two hours. 3,3,3-Trifluoropropyltrimethoxysilane (45 mmol) was added via pressure equalizing addition funnel. The contents were brought to reflux (65-70° C.) for two hours, and reaction progress was monitored by GC. Isolation was accomplished by removing the THF via rotary evaporation, taking the residue up in ether (250 mL), filtration and ether removal via rotary evaporation. Purification was accomplished by distillation to provide 3,3,3-trifluoropropyl bis(2-ethylhexyl)aminodimethoxysilane (44 mmol; 98% yield). C21H44NO2SiF3 (mw=427.66) bp=200° C. at 1.4 mmHg; 1H NMR: (CDCl3) δ 3.5 (s, 6H), 2.6-2.4 (dd, 4H), 2.2-2.0 (m, 2H), 1.6-1.1 (m, 18H), 1.0-0.7 (m, 14H); 13C NMR: (CDCl3) δ 128 (quartet, J=275 Hz), 50.4, 48.5, 39.4, 36.9, 30.8, 29.1, 28.2 (quartet, J=30 Hz), 23.2, 14.2, 10.3, 3.2; MS: m/z (relative abundance) 328 (100), 230 (25.6), 155 (7.4), 109 (2.9).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06130180
出典データセットuspto-grants-2000_10
ORD IDord-01b6999923c54c6dbe7f38602d9dab81
出典メモuspto-grants-2000_10