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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796964Generated: November 1, 2026

Ethyl (2E)-3-ethoxy-2-butenoate → HCID 178488530, compound

https://huagongshe.com/reaction/1796964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (2E)-3-ethoxy-2-butenoateHCID 5354173—
Reactant2-(4-methoxy-2-methylphenyl)-3-methyl-1H-pyrrol-1-amineHCID 22174784—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventChloroformHCID 6212—
ProductHCID 178488530HCID 17848853065%

Reaction Steps

A mixture of 2-(4-methoxy-2-methylphenyl)-3-methyl-1H-pyrrol-1-amine (0.23 g, 1.06 mmol), ethyl trans-3-ethoxycrotonate (0.17 g, 1.06 mmol) and p-toluenesulfonic acid (0.01 g, 0.053 mmol) in CHCl3 (7.0 mL) was refluxed with a Dean-Stark tube charged with molecular sieves for 24 h. After cooling down to room temperature, the mixture was concentrated in vacuo to dryness and the residue was subjected to column chromatography (silica gel, 1/4 EtOAc/heptane) to give 0.194 g (65%) of beige foam as the desired product: mp 234–237° C.; 1H NMR (300 MHz, CDCl3) δ 7.22 (d, J=8 Hz, 1H), 6.89–6.87 (m, 1H), 6.84–6.79 (m, 1H), 6.54 (br s, 1H), 5.94 (br s, 1H), 3.85 (s, 3H), 2.34 (s, 3H), 2.18 (s, 3H), 2.08 (s, 3H); MS m/z 283.2 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034023B2
Source datasetuspto-grants-2006_04
ORD IDord-7d3adaae462e41e7bdac2c497441f05e
Source noteuspto-grants-2006_04