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HRID 335367作成日:2026年10月24日

Imidazole → 7-(Iodomethyl)pentadecane

https://huagongshe.com/ja/reaction/335367

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物IodineHCID 807—
反応物TriphenylphosphineHCID 11776—
反応物2-Hexyl-1-decanolHCID 95337—
溶媒DichloromethaneHCID 6344—
生成物7-(Iodomethyl)pentadecaneHCID 5809832382%

反応条件

温度0 °C

反応手順

Under air, triphenylphosphine (107.44 g, 410 mmol, 1.19 equiv.) and imidazole (28.9 g, 424 mmol, 1.23 equiv.) were dissolved in dichloromethane (800 mL). 2-Hexyl-1-decanol (100 mL, 345 mmol., 1.00 equiv.) was added to the solution, and the reaction mixture was cooled to 0° C. Iodine (103.6 g, 408 mmol., 1.18 equiv.) was added portion-wise over 1 hour, after which the suspension was stirred at 0° C. for an additional hour, and then at ambient temperature for 18 hours. The mixture was quenched with saturated aqueous Na2SO3 (150 mL), and DCM was removed in vacuo. Hexane (200 mL) was added to the residue, and the mixture was filtered to remove salts that had precipitated. The organic material was extracted with hexanes (3×300 mL), dried over Na2SO4, filtered through a pad of silica gel, and then concentrated in vacuo to give a clear, colorless oil (97.8 g, 82% yield). 1H NMR (500 MHz, CDCl3) δ 3.28 (d, J=4.6 Hz, 2H), 1.34-1.19 (m, 24H), 1.12 (b, 1H), 0.91-0.87 (m, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883958B2
出典データセットuspto-grants-2014_11
ORD IDord-ffb63b48f1d74257833af0c431c70c95
出典メモuspto-grants-2014_11