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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497520Generated: October 30, 2026

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

https://huagongshe.com/reaction/497520

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 numberUS06949573B2
Source datasetuspto-grants-2005_09
ORD IDord-f67384807d3e4a658540480532b37cbd
Source noteuspto-grants-2005_09