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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant4-Bromo-3-methoxyanilineHCID 7018254—
Reactantethyl (2Z)-3-(methylamino)-3-phenylacrylateHCID 10976613—
SolventDichloromethaneHCID 6344—
Productethyl (2Z)-3-[(4-bromo-3-methoxyphenyl)amino]-3-phenylacrylateHCID 5761709887.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879797B2
Source datasetuspto-grants-2011_02
ORD IDord-c446a2855e364668ba8487f6ba1bf70e
Source noteuspto-grants-2011_02