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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369825Generated: October 30, 2026

Imidazole → HCID 68803997, compound

https://huagongshe.com/reaction/2369825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactant4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-oneHCID 14121—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventEthyl AcetateHCID 8857—
ProductHCID 68803997HCID 6880399773%

Reaction Steps

To a solution of 4-(4-Hydroxy-3-methoxy-phenyl)but-3-ene-2-one (4.402 g, 22.93 mmol) in N,N-dimethylformamide (28.5 mL) were added imidazole (1.71 g, 25.22 mmol) and tert-butyldimethylsilyl chloride (3.8 g; 25.22 mmol). The reaction was allowed to stir for 4 h, then diluted with ethyl acetate (300 mL) and washed with water (50 mL), saturated aqueous sodium bicarbonate (40 mL), and saturated aqueous sodium chloride (50 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated at reduced pressure to give crude product. Column purification on silica (8:2 hexanes/ethyl acetate) afforded 4-{4-[(tert-butyl-dimethyl-silanyloxy)-methyl}-3-methoxy-phenyl}-but-3-ene-2-one (5.24 g, 73% yield) as a solid: 1H NMR (400 MHz, CDCl3): δ 7.32 (d, 2H), 6.92 (m, 2H), 6.78 (d, 1H), 6.53 (d, 2H), 3.78 (s, 3H), 2.28 (s, 3H), 0.92 (s, 9H), 0.16 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710038B2
Source datasetuspto-grants-2014_04
ORD IDord-973575e7ead14b91bb3fb835625e145b
Source noteuspto-grants-2014_04