HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360103Generated: October 30, 2026
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → ethyl (2Z)-3-[(4-bromo-3-methoxyphenyl)amino]-3-phenylacrylate
https://huagongshe.com/reaction/1360103
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 4-Bromo-3-methoxyaniline | HCID 7018254 | — |
| Reactant | ethyl (2Z)-3-(methylamino)-3-phenylacrylate | HCID 10976613 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl (2Z)-3-[(4-bromo-3-methoxyphenyl)amino]-3-phenylacrylate | HCID 57617098 | 87.3% |
Reaction Steps
To a solution of ethyl (2Z)-3-(methylamino)-3-phenylacrylate (4.47 g, 21.77 mmol) in DCM (100 mL) was added 4-bromo-3-methoxyaniline (4 g, 19.80 mmol) and PPTS (5.47 g, 21.77 mmol). The mixture was then heated to reflux for 24 h. At this time crude 1H NMR revealed nearly complete consumption of the aniline. The reaction was then cooled to RT, filtered, and the solvent was removed in vacuo. The crude product was purified on silica (75% DCM/hexanes) to yield ethyl (2Z)-3-[(4-bromo-3-methoxyphenyl)amino]-3-phenylacrylate (6.5 g, 87%) which was used as is in subsequent reactions. 1H NMR (500 MHz, CDCl3) ppm: 10.32 (br s, 1H), 7.32 (m, 5H), 7.20 (d, J=8.5 Hz, 1H), 6.19 (dd, J=8.5 Hz, 2.5 Hz, 1H), 6.11 (d, J=2.5 z, 1H), 5.03 (s, 1H), 4.21 (q, J=7.0 Hz, 2H), 3.50 (s, 3H), 1.32 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879797B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-c446a2855e364668ba8487f6ba1bf70e |
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| Source note | uspto-grants-2011_02 |
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