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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896393Generated: October 30, 2026

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

https://huagongshe.com/reaction/896393

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 numberUS06919324B2
Source datasetuspto-grants-2005_07
ORD IDord-8b1f9152f85d43c3a1c8991164d2c42d
Source noteuspto-grants-2005_07