HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712539Generated: October 26, 2026
Diisobutylaluminumhydride → [2-(3-Methoxypropyl)-1-(2-trimethylsilanylethoxymethyl)-1H-benzoimidazol-4-yl]methanol
https://huagongshe.com/reaction/1712539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 2-(3-methoxypropyl)-1-(2-trimethylsilanylethoxymethyl)-1H-benzoimidazole-4-carboxylate | HCID 68502641 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(3-Methoxypropyl)-1-(2-trimethylsilanylethoxymethyl)-1H-benzoimidazol-4-yl]methanol | HCID 68503680 | — |
Reaction Steps
35 ml of diisobutylaluminium hydride (1.5M in toluene) are added dropwise at −70° C. to a solution of 4.95 g of methyl 2-(3-methoxypropyl)-1-(2-trimethylsilanylethoxymethyl)-1H-benzoimidazol-4-carboxylate in 200 ml of tetrahydrofuran. The reaction mixture is then stirred at −10° C. for 1 hour and subsequently partitioned between tert-butyl methyl ether and 2:1 water/1N potassium bisulphate solution—the organic phase is washed with saturated aqueous sodium bicarbonate solution and water, dried over sodium sulphate and concentrated by evaporation. The combined aqueous phases are reextracted with ethyl acetate (3×)—the combined organic phases are washed with saturated aqueous sodium bicarbonate solution and water, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a yellow oil from the residues by means of flash chromatography (SiO2 60F). Rf=021 (95:5 ethyl acetate-methanol), Rt=3.91.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790715B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-03cc4c751a434cd5813f3c313f89ed94 |
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| Source note | uspto-grants-2010_09 |
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