Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244340Generated: October 30, 2026

Water → 3-[2-(2-Bromo-5-fluoro-phenoxymethyl)-phenyl]-acrylic acid ethyl ester

https://huagongshe.com/reaction/244340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcrylateHCID 8821—
ReactantSodium AcetateHCID 517045—
Reactant1-Bromo-4-fluoro-2-(2-iodo-benzyloxy)-benzeneHCID 58564425—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Solventtert-Butyl methyl etherHCID 15413—
Product3-[2-(2-Bromo-5-fluoro-phenoxymethyl)-phenyl]-acrylic acid ethyl esterHCID 6713344395%

Reaction Steps

To a mixture of 1-bromo-4-fluoro-2-(2-iodo-benzyloxy)-benzene (117.4 g, 0.29 mol), sodium acetate (36.1 g, 0.44 mol), tetra-n-butylammonium bromide (90.3 g, 0.29 mol), palladium (II) acetate (1.8 g, 8 mmol, 3 mol %), and N-methylpyrrolidinone (900 mL) at 55-60° C., add dropwise a solution of ethyl acrylate (34.3 mL, 0.32 mol) in N-methylpyrrolidinone (200 mL). Cool the reaction mixture to room temperature and treat with water (2 L) and methyl tert-butyl ether (2 L). Pass the reaction through diatomaceous earth, add ethyl acetate (1 L), separate the layers, and wash with water (2 L). Dry the organic portion over anhydrous sodium sulfate, filter, and concentrate. Suspend the resulting solid in hexanes (1 L), refrigerate for 2 h, filter, and wash with cold hexanes (500 mL). Dry in a vacuum oven (50° C./20 mm Hg) to obtain the title compound as a pale yellow solid (104.4 g, 95%). LC-MS m/z 381.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658638B2
Source datasetuspto-grants-2014_02
ORD IDord-4e33039bc6054fbf846988590793f18d
Source noteuspto-grants-2014_02