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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295907Generated: October 30, 2026

Imidazole → 4-[(Tert-butyldimethylsilyl)oxy]-2-chlorobenzaldehyde

https://huagongshe.com/reaction/1295907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Chloro-4-hydroxybenzaldehydeHCID 185363—
SolventDimethylformamideHCID 6228—
Product4-[(Tert-butyldimethylsilyl)oxy]-2-chlorobenzaldehydeHCID 5890746975%

Reaction Steps

A solution of 2-chloro-4-hydroxybenzaldehyde (5.0 g, 32 mmol), tert-butyl(dimethyl)silyl chloride (5.3 g, 35 mmol), imidazole (2.9 g, 45 mmol) and N,N-dimethylaminopyridine (10 mg) in N,N-dimethylformamide (40 ml) was stirred at room temperature under a nitrogen atmosphere for 16 hours. The solvent was removed in vacuo and the residue partitioned between ethyl acteate (100 ml) and water (100 ml). The organic phase was separated, washed with sat. aq. sodium chloride (50 ml), dried (sodium sulfate) and reduced in vacuo. Further purification by column chromatography on silica gel eluting with pentane:ethyl acetate (3:1 changing to 2:1) gave the title compound as a colourless oil (6.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244766B2
Source datasetuspto-grants-2007_07
ORD IDord-fd507c1fbf134d1293ebfd7e050cb1be
Source noteuspto-grants-2007_07