HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276035Generated: October 26, 2026
Sodium Sulfate → 1h-Benzimidazole-6-methanol,1-[(2-chlorophenyl)methyl]-2-methyl-
https://huagongshe.com/reaction/276035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 1-(2-Chlorobenzyl)-6-ethoxycarbonyl-2-methylbenzimidazole | HCID 18680839 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Lithium ammonium hydride | HCID 86650320 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1h-Benzimidazole-6-methanol,1-[(2-chlorophenyl)methyl]-2-methyl- | HCID 18315538 | 62.5% |
Reaction Steps
A solution of 2.66 g of 1-(2-chlorobenzyl)-6-ethoxycarbonyl-2-methylbenzimidazole in 20 ml of tetrahydrofuran was slowly added to a solution of 1.54 g of lithium aluminum hydride in 20 ml of tetrahydrofuran at a temperature of from 20 to 25° C. Further, the mixture was stirred at room temperature for 1 hour. Thirty milliliters of tetrahydrofuran were added thereto to dilute the reaction solution. Lithium ammonium hydride was decomposed and solidified with a saturated aqueous solution of sodium sulfate, and the tetrahydrofuran layer was separated. The solvent was distilled off, and the residue was purified through silica-gel column chromatography (eluent: a mixture of chloroform and methanol at a ratio of 9:1) to give 1.45 g of 1-(2-chlorobenzyl)-6-hydroxymethyl-2-methylbenzimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352985B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-b9780ffbde374e5eafda12e93553ae47 |
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| Source note | uspto-grants-2002_03 |
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