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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339578Generated: October 31, 2026

Water → (2-Bromoethoxy)-tert-butyldimethylsilane

https://huagongshe.com/reaction/339578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantEthanol, 1-bromo-HCID 14202443—
SolventDichloromethaneHCID 6344—
Product(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 360806755%

Reaction Steps

To a stirred solution of bromoethanol (9.912 g, 79.32 mmol) in dry DCM (25 ml) was added in one portion tert-butyldimethylsilyl chloride (13.212 g, 85.03 mmol) and the reaction mixture stirred at room temperature. A solution of triethylamine (8.865 g, 12.3 ml, 87.61 mmol) in dry DCM (40 ml) was then added dropwise over 1 h and 20 min. The reaction mixture was stirred at room temperature for 3 d, then water (30 ml) was added. The organic phase was separated and the aqueous phase was extracted with DCM (2×20 ml). The combined organic extracts were washed with brine (30 ml), dried (Na2SO4), and the solvent removed under reduced pressure to give a pale yellow oil. Distillation under reduced pressure gave the title compound (10.54 g, 55%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-e74c3a8f85c2458d90b74ff5893aee3b
Source noteuspto-grants-2014_11