HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108063Generated: October 26, 2026
Methanol → [4-(2-Methylimidazol-1-yl)phenyl]methanol
https://huagongshe.com/reaction/1108063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Ethyl 4-(2-methyl-1H-imidazol-1-yl)benzoate | HCID 14664350 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [4-(2-Methylimidazol-1-yl)phenyl]methanol | HCID 11735617 | 95% |
Reaction Steps
To a solution of ethyl 4-(2-methylimidazol-1-yl)benzoate (46 g, 0.2 mol) in dry CH2Cl2 (1 l) cooled to -75° C. under a nitrogen atmosphere was added diisobutyl-aluminum hydride (540 ml, 0.93 M in hexane) carefully over 30 minutes and then the mixture was allowed to warm slowly to ambient temperature. After stirring for 5 hours the reaction mixture was cooled in an ice-bath and methanol (30 ml) carefully added. A 30% aqueous solution of Rochelle's salt (500 ml) was then added and the mixture stirred at ambient temperature for 16 hours. Insolubles (essentially product) were removed by filtration and the organic phase separated and washed with water (500 ml), dried (MgSO4) and evaporated. The combined resultant solids were recrystallized from ethanol (ca 300 ml) to afford the titled compound (35.6 g, 95%) as white needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06063928 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-023c92e845624906a88a32ef8ca33974 |
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| Source note | uspto-grants-2000_05 |
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