Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415483Generated: November 1, 2026

Water → (Z)-3-(4-bromo-3-methoxy-phenylamino)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/2415483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetoacetateHCID 8868—
Reactant4-Bromo-3-methoxyanilineHCID 7018254—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventCyclohexaneHCID 8078—
Product(Z)-3-(4-bromo-3-methoxy-phenylamino)-but-2-enoic acid ethyl esterHCID 6928716668.9%

Reaction Steps

7.66 g (37.9 mmol) of 4-bromo-3-methoxy-phenylamine (preparation described in Tetrahedron Lett., 1995, 7583) were dissolved in 80 ml of cyclohexane at 70° C. and subsequently treated under stirring with 72 mg (0.38 mmol) of p-toluenesulfonic acid monohydrate and 4.93 g (37.9 mmol) of ethyl acetoacetate. The solution was then heated at reflux for 3.5 h with a water separator funnel connected. It was then cooled to RT and concentrated in vacuo. The residue was applied to a silica gel column with hexane/diethyl ether (3:1) as eluent. Combinations of the purified fractions and concentration in vacuo gave 8.2 g (68.8%) of the (Z)-3-(4-bromo-3-methoxy-phenylamino)-but-2-enoic acid ethyl ester, as a yellow solid. ISP mass spectrum, m/e: 316.2(M+1 calculated for C13H16BrNO3: 316).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818767B2
Source datasetuspto-grants-2004_11
ORD IDord-e6c9897c8f6d498fb4fa75927f0a7fee
Source noteuspto-grants-2004_11