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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420438Generated: October 31, 2026

Imidazole → (2-Bromoethoxy)-tert-butyldimethylsilane

https://huagongshe.com/reaction/420438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactant2-BromoethanolHCID 10898—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 360806797%

Reaction Steps

Following a published procedure, 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097609B2
Source datasetuspto-grants-2012_01
ORD IDord-eaef83b180024fd2aae7e6159e5c3ee9
Source noteuspto-grants-2012_01