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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497519Generated: October 30, 2026

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

https://huagongshe.com/reaction/497519

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDichloromethaneHCID 6344—
Product3-(t-Butyldimethylsilyloxy)benzaldehydeHCID 1120711192.4%

Reaction Steps

3-Hydroxybenzaldehyde (5.14 g, 42.1 mmol) was added to a suspension of tert-butyl-dimethyl-silyl chloride (6.7 g, 44.4 mmol) and imidazole (3.03 g, 44.5 mmol) in dichloromethane (100 ml) under an atmosphere of nitrogen at room temperature. The reaction mixture was stirred at room temperature for 18 hours, and the mixture washed sequentially with 1 M hydrochloric acid (2-fold 50 ml) followed by a saturated aqueous solution of sodium hydrogen carbonate (50 ml). The organic phase was separated, dried over anhydrous magnesium sulphate and the solvent removed in vacuo. The residual yellow oil was passed through a plug of silica gel eluting with 1:1, by volume, dichloromethane:pentane giving 3-(tert-butyl-dimethyl-silanyloxy)-benzaldehyde (9.2 g) as a golden yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949573B2
Source datasetuspto-grants-2005_09
ORD IDord-e690ce280ca544a89e37cac13711a0e1
Source noteuspto-grants-2005_09