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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089676Generated: October 31, 2026

Triethylamine → Tert-butyl(2-fluoro-5-methoxyphenoxy)dimethylsilane

https://huagongshe.com/reaction/2089676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Fluoro-5-methoxyphenolHCID 14118957—
SolventTetrahydrofuranHCID 8028—
SolventHeptaneHCID 8900—
ProductTert-butyl(2-fluoro-5-methoxyphenoxy)dimethylsilaneHCID 6746996194.7%

Reaction Steps

To a flask, 2-fluoro-5-methoxyphenol (6.00 g, 42 mmol), triethylamine (5.77 g, 57 mmol), and tetrahydrofuran (36.0 mL) were added, and the resulting mixture was cooled in an ice water bath under nitrogen atmosphere. To the solution, a solution of tert-butyldimethylsilyl chloride (6.89 g, 44 mmol) in tetrahydrofuran (30.0 mL) was added dropwise, and the resulting mixture was stirred overnight at room temperature. To the reaction mixture, heptane and a 2 N aqueous sodium hydroxide solution were added, and the resulting mixture was extracted. The organic layer was washed with water, and concentrated under reduced pressure to obtain the captioned compound (10.2 g) as a light brownish-red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436009B2
Source datasetuspto-grants-2013_05
ORD IDord-33c135b237134441b736a2e66c26860e
Source noteuspto-grants-2013_05