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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054174Generated: November 2, 2026

Potassium Carbonate → Ethyl (2E)-4-(5-bromo-2-nitrophenoxy)but-2-enoate

https://huagongshe.com/reaction/1054174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl (E)-4-bromobut-2-enoateHCID 5373944—
Reactant5-Bromo-2-nitrophenolHCID 13970496—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl (2E)-4-(5-bromo-2-nitrophenoxy)but-2-enoateHCID 13173633199%

Reaction Steps

5-Bromo-2-nitrophenol (10 g, 45.9 mmol) and K2CO3 (8.24 g, 59.6 mmol) were suspended in NMP (81 mL) (a bright red suspension) and ethyl 4-bromocrotonate (10.26 mL, 59.63 mmol) was added dropwise at room temperature. The reaction was stirred at room temperature over night (20 h). The mixture was poured into ice/water (500 mL) and stirred for 30 min. The precipitate was collected by filtration and washed with water (2×200 mL), air dried for 10 min and then washed with heptane (200 mL). Heptane (200 mL) was added to the solid and stirred for 1 h. The solid was filtered off, washed with heptane (2×50 mL) and dried in vacuo to afford a beige solid. The title compound (15.0 g, 99%) was obtained and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394291B2
Source datasetuspto-grants-2016_07
ORD IDord-0fa0ccfe2a234a8e9979fc65f6f0fb09
Source noteuspto-grants-2016_07