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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374777Generated: October 30, 2026

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

https://huagongshe.com/reaction/1374777

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 numberUS07166589B2
Source datasetuspto-grants-2007_01
ORD IDord-5689835f00dc4779903741eb58ac23f9
Source noteuspto-grants-2007_01