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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505776Generated: October 30, 2026

Benzaldehyde → Methyl 4-nitro-5-[(E)-2-phenylethenyl]thiophene-2-carboxylate

https://huagongshe.com/reaction/505776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPyrrolidineHCID 31268—
ReactantMethyl 5-methyl-4-nitrothiophene-2-carboxylateHCID 268679—
SolventMethanolHCID 887—
ProductMethyl 4-nitro-5-[(E)-2-phenylethenyl]thiophene-2-carboxylateHCID 1151478567%

Reaction Steps

A solution (0.33 M) of methyl 5-methyl-4-nitrothiophene-2-carboxylate in MeOH, was treated with benzaldehyde (1.5 eq.). The reaction mixture was heated to reflux and when it became a clear solution a catalytic amount of pyrrolidine (0.01 eq.) was added. After 18 h at reflux additional pyrrolidine (0.01 eq.) was added. The reaction was heated to reflux for 40 h. After cooling down, evaporation of the solvent gave a residue that was purified by flash chromatography on silica gel (1:9 AcOEt/petroleum ether) to afford the title compound (67%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781431B2
Source datasetuspto-grants-2010_08
ORD IDord-0dbdf03c2e934233833547dbb1506e68
Source noteuspto-grants-2010_08