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HRID 40532作成日:2026年10月23日

Imidazole → (2-Bromoethoxy)-tert-butyldimethylsilane

https://huagongshe.com/ja/reaction/40532

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物WaterHCID 962—
反応物2-BromoethanolHCID 10898—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 360806797%

反応手順

Following a published procedure,24 2-bromoethanol (10.0 mL, 141 mmol) was added to a mixture of imidazole (12.5 g, 184 mmol) and tert-butyldimethylsilyl chloride (21.1 g, 140 mmol) in anhydrous DMF (25 mL). The reaction mixture was stirred at room temperature for 12 h. Water and diethyl ether were added. The phases were separated. The aqueous phase was extracted with diethyl ether. The combined organic phases were washed with water and brine. The solution was dried (Na2SO4). Evaporation of the solvent followed by bulb-to-bulb distillation (40-45° C./0.05 mmHg) yielded a colorless liquid (32.5 g, 97%): IR (film, νmax cm−1) 2951, 2859, 1471; 1H NMR δ 0.07 (s, 6H), 0.89 (s, 9H), 3.36-3.41 (m, 2H), 3.85-3.90 (m, 2H); 13C NMR δ −5.06, 18.49, 26.04, 33.45, 63.74; EI-MS 137/139, 181/183, calcd 238.0389 (C8H19BrOSi); Anal. Calcd C, 40.17; H, 8.01. Found: C, 40.55; H, 8.25.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530459B2
出典データセットuspto-grants-2013_09
ORD IDord-92442a17ea5244309ef8f7e03d77d7bd
出典メモuspto-grants-2013_09