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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714931Generated: October 30, 2026

Triethylamine → Ethyl 2-bromo-3-(4-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/714931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantBenzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 76150—
ReactantPyridinium hydrobromideHCID 21226041—
SolventEthanolHCID 702—
ProductEthyl 2-bromo-3-(4-methoxyphenyl)-3-oxopropanoateHCID 1304836089%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl p-anisoylacetate (1.00 g, 4.5 mmol) in ethanol (14 mL) at 50° C. was added triethylamine (0.63 mL, 4.5 mmol) followed by pyridinium hydrobromide perbromide (1.44 g, 4.5 mmol) and the resulting mixture was then stirred at 50° C. for 2 hours. The reaction was cooled to room temperature and poured into EtOAc. The organic phase was then washed with saturated sodium bicarbonate solution and 0.5M aqueous HCl, dried over MgSO4 and the solvent removed in vacuo to afford ethyl 2-bromo-3-(4-methoxyphenyl)-3-oxopropanoate (1.209 g, 4.0 mmol, 89%) which was used without further purification. 1H NMR (CDCl3) δ 1.26 (3H, t), 3.89 (3H, s), 4.28 (2H, q), 5.62 (1H, s), 6.96 (2H, d), 7.98 (2H, d). LCMS (2) Rt: 3.06 min; m/z (ES+) 301/303.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-b055093532a44040bed4c968f6ef12d4
Source noteuspto-grants-2015_11