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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222565Generated: October 30, 2026

Imidazole → (2-Bromoethoxy)(tert-butyl)diphenylsilane

https://huagongshe.com/reaction/222565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-BromoethanolHCID 10898—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product(2-Bromoethoxy)(tert-butyl)diphenylsilaneHCID 10915442101.1%

Reaction Steps

A mixture of tert-butyldiphenylsilyl chloride (20.32 g, 74.03 mmol) and imidazole (6.25 g, 91.9 mmol) was treated dropwise with 2-bromoethanol (47, 5 mL, 8.87 g, 70.8 mmol). Stirring was continued for 12 h. The mixture was diluted with Et2O and water. The phases were separated, and the aqueous layer was extracted Et2O. The organic extract was washed with water and dried over Na2SO4. Concentration of the sample yielded a pale brown oil (26.01 g, 97%): 1H NMR δ 1.11 (s, 9H), 3.45 (t, J=6.3 Hz, 2H), 3.96 (t, J=6.3 Hz, 2H), 7.42-7.47 (m, 6H), 7.70-7.73 (m, 4H); 13C NMR δ 19.52, 27.03, 33.43, 64.24, 128.04, 130.10, 133.49, 135.84.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207329B2
Source datasetuspto-grants-2012_06
ORD IDord-c2f320f3e7f540439c86fa6a8d97a74d
Source noteuspto-grants-2012_06