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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131092Generated: October 31, 2026

tert-Butyldimethylsilyl chloride → 2-(t-Butyldimethylsilyl)-3-bromo-4-methoxy benzaldehyde

https://huagongshe.com/reaction/131092

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-Bromo-2-hydroxy-4-methoxybenzaldehydeHCID 14120945—
SolventDimethylformamideHCID 6228—
Product2-(t-Butyldimethylsilyl)-3-bromo-4-methoxy benzaldehydeHCID 2234925683.1%

Reaction Steps

Diiospropylethylamine (3.0 ml) was added to a stirred solution (under argon) of 2-hydroxy-3-bromo- -4-methoxybenzaldehyde (1.96, 8.5 mmole) in DMF (15 ml) followed by t-butyldimethlsilyl chloride (TBSCl, 1.91 g, 12.8 mmole). The reaction mixture was stirred at room temperature for 30 min and Ice (20 g) was added to the mixture. The mixture was then extracted with ether (3×25 ml). The ethereal solution was washed with water (25 ml) and saturated NaHCO3 solution (2×15 ml). The solvent evaporated to yield 2-(t-butyldimethylsilyl)-3-bromo-4-methoxy benzaldehyde as an oil (2.54 g, 7.06 mmole, 83.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384925B2
Source datasetuspto-grants-2008_06
ORD IDord-705325ef04a849a39f8f6379eeb183ef
Source noteuspto-grants-2008_06