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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium sulfate decahydrateHCID 62649—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 1-(4-benzyloxybenzyl)-4-phenylpyrrole-3-carboxylateHCID 23024961—
SolventTetrahydrofuranHCID 8028—
Product[1-(4-Benzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanolHCID 2302509798.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-09d6ae465fc24d6e9337f9e4b92d37a2
Source noteuspto-grants-2007_02