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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3602Generated: October 23, 2026

Pyrrole-2-carboxaldehyde → 1-[2-Nitro-5-(ethoxycarbonyl)benzyl]-pyrrole-2-carboxaldehyde

https://huagongshe.com/en/reaction/3602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromomethyl-4-nitro-benzoic acid ethyl esterHCID 13077445—
SolventTetrahydrofuranHCID 8028—
Product1-[2-Nitro-5-(ethoxycarbonyl)benzyl]-pyrrole-2-carboxaldehydeHCID 2183711583.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred slurry of 2.2 g of sodium hydride (60% in oil, washed with hexane) in tetrahydrofuran is added at 0° C. a solution of 4.5 g of pyrrole-2-carboxaldehyde in 25 ml of tetrahydrofuran. After the addition is complete, a solution of 15 g of ethyl 4-nitro-3-bromomethylbenzoate in 30 ml of dry tetrahydrofuran is slowly added under nitrogen. The reaction mixture is stirred at 20° C. for 8 hours and carefully quenched with water. The reaction mixture is extracted with chloroform which is washed with water, dried with Na2SO4 and concentrated in vacuo to give 12 g of the desired product as a solid; mass spectrum (M+ H)349.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733905
Source datasetuspto-grants-1998_03
ORD IDord-169b2f504f264086a66d2edfe51fb873
Source noteuspto-grants-1998_03