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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746024Generated: November 2, 2026

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

https://huagongshe.com/reaction/1746024

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 numberUSRE045720E1
Source datasetuspto-grants-2015_10
ORD IDord-9f1da921f36d4e47a7d9e2469f6690fd
Source noteuspto-grants-2015_10