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HRID 2066667作成日:2026年10月27日

Potassium Carbonate → Tert-butyl(dimethyl)[(2-{[4-(trifluoromethoxy)phenoxy]methyl}-2-propenyl)oxy]silane

https://huagongshe.com/reaction/2066667

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物p-(Trifluoromethoxy)phenolHCID 70015—
反応物Tert-butyl(dimethyl)silyl 2-(iodomethyl)-2-propenyl etherHCID 11358863—
溶媒AcetoneHCID 180—
生成物Tert-butyl(dimethyl)[(2-{[4-(trifluoromethoxy)phenoxy]methyl}-2-propenyl)oxy]silaneHCID 6695567058.2%

反応条件

温度50 °C

反応手順

A mixture of iodide 165 (4.63 g, 14.8 mmol), 4-(trifluoromethoxy)phenol (3.10 mL, 23.9 mmol) and powdered K2CO3 (3.56 g, 25.8 mmol) in acetone (10 mL) was stirred at 50° C. for 11 h. The resulting cooled mixture was diluted with ice-water (100 mL) and extracted with CH2Cl2 (4×100 mL). The combined extracts were evaporated to dryness and the residue was chromatographed on silica gel. Elution with 0-3% CH2Cl2/petroleum ether firstly gave foreruns, and then further elution with 5-10% CH2Cl2/petroleum ether gave tert-butyl(dimethyl)[(2-{[4-(trifluoromethoxy)phenoxy]methyl}-2-propenyl)oxy]silane (166) (3.12 g, 58%) as a colourless oil; 1H NMR (CDCl3) δ 7.12 (br d, J=9.0 Hz, 2H), 6.90 (dt, J=9.1, 2.9 Hz, 2H), 5.27 (d, J=0.7 Hz, 1H), 5.20 (d, J=1.1 Hz, 1H), 4.54 (s, 2H), 4.24 (s, 2H), 0.91 (s, 9H), 0.07 (s, 6H); HRFABMS calcd for C17H26F3O3Si m/z [M+H]+ 363.1603. found 363.1604.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08293734B2
出典データセットuspto-grants-2012_10
ORD IDord-437284d6566449988b6d308e5a93464c
出典メモuspto-grants-2012_10