Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622126Generated: October 31, 2026

4-Methoxystyrene → HCID 21293332, compound

https://huagongshe.com/reaction/622126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxystyreneHCID 12507—
Reactant2-Chloroethyldiisopropylammonium chlorideHCID 77942—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
ReactantHCID 17846762HCID 17846762—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethyl SulfoxideHCID 679—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
ProductHCID 21293332HCID 21293332—

Reaction Conditions

Temperature60 °C

Reaction Steps

6-Bromo-2-[2-(dimethyamino)ethyl]phthalazin-1(2H)-one (7.2 gm, 0.018 mole) (prepared as in Example I, except that 2-(dimethylamino)ethyl chloride hydrochloride was substituted for the 2-(diisopropylamino)ethyl chloride hydrochloride) was stirred into 16 ml DMSO plus 16 ml acetonitrile. To the resulting mixture was added 4.5 gm 4-methoxystyrene (0.033 mole), 0.1 gm tri(o-tolyl)phosphine, and 0.02 gm palladium acetate. The reaction mixture was stirred at reflux (95°-100° C.) for 24 hours. Allowed to cool to about 60° C. and diluted with 60 ml of isopropanol. Stirred for an hour, filtered, washed to colorless washings with isopropanol and dried. The product weighed 10.7 gm. After recrystallization from 240 ml methoxyethanol the product weighed 6.4 gm and melted at 265°-267° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04769369
Source datasetuspto-grants-1988_09
ORD IDord-4e212aaf2d024257a85b02ab13d8edc1
Source noteuspto-grants-1988_09