Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504401Generated: October 26, 2026

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → (E)-ethyl 3-(5-(benzylthio)-2-((4-bromo-5-fluoro-2-methoxyphenyl)amino)phenyl)-acrylate

https://huagongshe.com/reaction/1504401

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantSodium t-butoxideHCID 23676156—
Reactant1-Bromo-2-fluoro-4-iodo-5-methoxybenzeneHCID 71656157—
Reactant(E)-Ethyl 3-(2-amino-5-(benzylthio)phenyl)acrylateHCID 117740420—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(E)-ethyl 3-(5-(benzylthio)-2-((4-bromo-5-fluoro-2-methoxyphenyl)amino)phenyl)-acrylateHCID 11774684448.6%

Reaction Conditions

Temperature130 °C

Reaction Steps

A screw cap vial was charged with (E)-ethyl 3-(2-amino-5-(benzylthio)phenyl)acrylate (0.500 g, 1.595 mmol), xantphos (0.185 g, 0.319 mmol), Pd2(dba)3 (0.146 g, 0.160 mmol), sodium tert-butoxide (0.153 g, 1.595 mmol) and toluene (7.98 ml). The vial was purged with Argon, sealed and heated to 130° C. for 10 minutes. The reaction was cooled to RT and 1-bromo-2-fluoro-4-iodo-5-methoxybenzene (0.581 g, 1.755 mmol) was added and the reaction was continued heating at 100° C. for an additional 30 minutes. The reaction was cooled to RT, diluted with water and extracted with DCM (3×). The combined organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated. The resulting material was concentrated, dissolved in minimal DCM and purified via column chromatography (silica gel 40 g, gradient elution 0 to 50% EtOAc:Heptane) to afford 0.40 g of (E)-ethyl 3-(5-(benzylthio)-2-((4-bromo-5-fluoro-2-methoxyphenyl)amino)phenyl)acrylate (0.400 g, 0.775 mmol, 48.6% yield). m/z (ESI) 471.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-3ccdbba5f82e4fd4ab5fbad0fa98ac27
Source noteuspto-grants-2015_12