HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349887Generated: October 31, 2026
Hexane → [1-(4-Benzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol
https://huagongshe.com/reaction/349887
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 1-(4-benzyloxybenzyl)-4-phenylpyrrole-3-carboxylate | HCID 23024961 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1-(4-Benzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol | HCID 23025097 | 98.4% |
Reaction Steps
Lithium aluminium hydride (2.53 g) was added to a solution of methyl 1-(4-benzyloxybenzyl)-4-phenylpyrrole-3-carboxylate (21.52 g) in tetrahydrofuran (100 ml) at 0° C., and the mixture was stirred at room temperature for one hour. Sodium sulfate decahydrate (30.00 g) and hexane (100 ml) were added to the reaction mixture and the mixture was stirred at room temperature for one hour. After the precipitate was removed by filtration, the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and [1-(4-benzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol (19.68 g, yield: 98%) was obtained as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 122–123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179823B1 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-09d6ae465fc24d6e9337f9e4b92d37a2 |
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| Source note | uspto-grants-2007_02 |
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