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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021672Generated: October 31, 2026

Triethylamine → (2-Bromoethoxy)-tert-butyldimethylsilane

https://huagongshe.com/reaction/1021672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoethanolHCID 10898—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 360806762.4%

Reaction Steps

To a solution of 2-bromoethanol (5.0 g, 40.3 mmol) in DCM (20 mL) was added tert-butyldimethylsilyl chloride (9.1 g, 60.5 mmol) followed by the additions of triethylamine (8.14 g, 80.6 mmol) and 4-dimethylaminopyridine (49.2 mg, 0.4 mmol). The mixture was stirred at room temperature for 15 h and concentrated in vacuo. The residue was partitioned between 1N HCl and ethyl acetate. The aqueous portion was extracted with ethyl acetate. The combined organic portion was washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford yellow oil, which was purified by column chromatography eluting with PE:EA (50:1) to afford 123a as colorless oil (6.0 g, 62.4%). LCMS: (M+H)+ 241.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716274B2
Source datasetuspto-grants-2014_05
ORD IDord-209a46f390cc4e5e927c24e6e807ba9f
Source noteuspto-grants-2014_05