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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460110Generated: October 31, 2026

3-Hydroxybenzaldehyde → 3-(t-Butyldimethylsilyloxy)benzaldehyde

https://huagongshe.com/reaction/1460110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDimethylformamideHCID 6228—
Product3-(t-Butyldimethylsilyloxy)benzaldehydeHCID 1120711176%

Reaction Steps

A solution of 3-hydroxy benzaldehyde (183.6 g, 1.50 mol), tert-butylchlorodimethylsilane (227.6 g, 1.50 mol), and imidazole (255.4 g, 3.75 mol) in 700 mL of dimethylformamide was stirred overnight at room temperature. The reaction solution was poured into 1700 mL of water and extracted with three 350 mL portions of diethyl ether. The combined ether extracts were washed with two 350 mL portions of 1.0M sodium hydroxide, 350 ml of water, and 350 mL of saturated aqueous sodium chloride. The ether solution was dried over sodium sulfate and the solvent removed to give 268 g (76%) of 3-(tert-butyldimethylsilyloxy)benzaldehyde as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854249
Source datasetuspto-grants-1998_12
ORD IDord-cd2e321a8ae04e2c96019f188ff5b59b
Source noteuspto-grants-1998_12