HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207306Generated: October 31, 2026
Sodium hydride → 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehyde
https://huagongshe.com/reaction/2207306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehyde | HCID 13600235 | 72.3% |
Reaction Steps
An oily suspension of 20.8 g sodium hydride in mineral oil (50%, 0.52 mol) was washed mineral oil free by stirring with hexane 3-times and suspended in 400 ml DMF. Under stirring at ambient temperature 50.0 g (0.520 mol) imidazole-2-carbaldehyde was added to the suspension. After 1.5 h, 101 ml (0.572 mol) 2-(trimethylsilanyl)ethoxymethyl chloride was added and the reaction was stirred a further hour. Then excess water was added to the suspension and the reaction mixture was extracted three times with ethyl acetate. The organic phase was dried over Na2SO4 and the solvent was evaporated off under reduced pressure. The raw material was then purified by column chromatography (DCM) to yield 85.0 g (0.376 mol) of the SEM-protected imidazole-2-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376432B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-cb578041c017468fb81f18a570d43d8a |
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| Source note | uspto-grants-2016_06 |
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