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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743934Generated: October 30, 2026

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

https://huagongshe.com/reaction/1743934

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 numberUS07012073B2
Source datasetuspto-grants-2006_03
ORD IDord-bba279d1004342119e4d387642eb095a
Source noteuspto-grants-2006_03