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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828831Generated: November 1, 2026

Imidazole → Benzaldehyde, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

https://huagongshe.com/reaction/1828831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSalicylaldehydeHCID 6998—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDichloromethaneHCID 6344—
ProductBenzaldehyde, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-HCID 1090063586.4%

Reaction Steps

2-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 then 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 2-(tert-butyl-dimethyl-silanyloxy)-benzaldehyde (8.6 g) as a golden yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060717B2
Source datasetuspto-grants-2006_06
ORD IDord-43db196f74694305b2777f8006805737
Source noteuspto-grants-2006_06