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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829773Generated: October 31, 2026

Ethyl Acetoacetate → 3-(3-Benzyloxy-4-bromo-phenylamino)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/1829773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
Reactant3-(Benzyloxy)-4-bromoanilineHCID 14659501—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventCyclohexaneHCID 8078—
Product3-(3-Benzyloxy-4-bromo-phenylamino)-but-2-enoic acid ethyl esterHCID 69472459106.2%

Reaction Steps

To a mixture of 3-benzyloxy-4-bromo-phenylamine (55.7 g, 0.168 mol) and ethyl acetoacetate (23.4 mL, 0.185 mol) in cyclohexane was added toluene-4-sulfonic acid monohydrate (0.320 g, 1.68 mmol) The reaction mixture was refluxed during 6 h and the water was azeotropically removed. The reaction mixture was then partitioned between ethyl acetate and an aqueous solution of sodium hydrogenocarbonate. The organic layer was washed with brine, dried over sodium sulfate, filtered and the solvents were evaporated under vacuum. 69.6 g of the title compound were obtained. Black oil, ISP-MS: m/e=392.2 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064134B2
Source datasetuspto-grants-2006_06
ORD IDord-efc92bd078084cfa99170fc0548d195c
Source noteuspto-grants-2006_06