HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl (2E)-3-ethoxy-2-butenoate → HCID 178488530, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl (2E)-3-ethoxy-2-butenoate | HCID 5354173 | — |
| Reactant | 2-(4-methoxy-2-methylphenyl)-3-methyl-1H-pyrrol-1-amine | HCID 22174784 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178488530 | HCID 178488530 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07034023B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-7d3adaae462e41e7bdac2c497441f05e |
| Source note | uspto-grants-2006_04 |