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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366175Generated: November 1, 2026

Triethylamine → 4-Bromo-2-((tert-butyldimethylsilyl)oxy)-6-methylpyridine

https://huagongshe.com/reaction/1366175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 178422452HCID 178422452—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-((tert-butyldimethylsilyl)oxy)-6-methylpyridineHCID 59023043—

Reaction Steps

A solution of 4-bromo-6-methylpyridin-2-ol (376 mg, 2 mmol) in dry DMF (20 mL) is stirred under N2. TBDMS-Cl (600 mg, 4 mmol) is added, followed by triethylamine (0.97 mL, 7.00 mmol), and the mixture is stirred at rt for 1 h. The solution is poured into ice-water (170 mL) and extracted with diethyl ether (5×50 mL). The combined extracts are dried over Na2SO4 and the solvent is evaporated under reduced pressure. The residue is taken up in pentane (50 mL), dried over Na2SO4 and the solvent evaporated again, to afford the crude title compound as a yellow oil. This is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893058B2
Source datasetuspto-grants-2011_02
ORD IDord-4ad3f4bde8b34b9c8ae97d495a4e1bf2
Source noteuspto-grants-2011_02