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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860095Generated: October 31, 2026

N-bromobutanimide → Ethyl 3-(3-bromo4-hydroxyphenyl)-2-phenoxypropionate

https://huagongshe.com/reaction/1860095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3-(4-hydroxyphenyl)-2-phenoxypropionateHCID 18625748—
SolventChloroformHCID 6212—
ProductEthyl 3-(3-bromo4-hydroxyphenyl)-2-phenoxypropionateHCID 1862587577.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

N-bromosuccinimide (1.12 g) was added to a solution of ethyl 3-(4-hydroxyphenyl)-2-phenoxypropionate (1.43 g), which is the product of reference example 4(c) in chloroform (20 ml) at ambient temperature. The mixture was stirred at 70° C. for 4 hour and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The ethyl acetate layer was separated and washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified via chromatography on silica gel column using hexane/ethyl acetate=4/1 as the eluant to afford the desired compound (1.41 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528525B1
Source datasetuspto-grants-2003_03
ORD IDord-5bd58bb5f8344a2ab587f222083a1c02
Source noteuspto-grants-2003_03