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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350029Generated: October 25, 2026

Hydrochloric Acid → Methyl 1-(4-benzyloxybenzyl)-4-phenylpyrrole-3-carboxylate

https://huagongshe.com/reaction/350029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4-Benzyloxybenzyl chlorideHCID 70042—
ReactantMethyl 4-phenyl-1H-pyrrole-3-carboxylateHCID 5142464—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-(4-benzyloxybenzyl)-4-phenylpyrrole-3-carboxylateHCID 2302496197%

Reaction Steps

Sodium hydride (60%, oily, 2.55 g) was added to a mixture of methyl 4-phenylpyrrole-3-carboxylate (11.61 g), 4-benzyloxybenzyl chloride (15.23 g) and N,N-dimethylformamide (100 ml) at 0° C., and the mixture was stirred for one hour. The reaction mixture was poured into dilute hydrochloric acid, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and then concentrated. The residue was subjected to silica gel column chromatography, and methyl 1-(4-benzyloxybenzyl)-4-phenylpyrrole-3-carboxylate (22.16 g, yield: 97%) was obtained from the fraction eluted with ethyl acetate-hexane (1:4, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 97–98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-160fdf1a69ab41f684c6ecb2ba79a8f1
Source noteuspto-grants-2007_02