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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380007Generated: November 3, 2026

M-Xylene → HCID 18956464, compound

https://huagongshe.com/reaction/2380007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-XyleneHCID 7929—
ReactantHCID 18956456HCID 18956456—
ReactantHCID 18956462HCID 18956462—
ReactantHCID 53640275HCID 53640275—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 18956464HCID 1895646481.5%

Reaction Steps

3-(2-Bromotetrafluoroethoxy)-N-(4-(2-bromotetrafluoroethoxy)phenyl)phthalimide Into a 250 ml round bottomed flask fitted with a mechanical stirrer and a Dean-Stark trap is placed 4-(2-bromotetrafluoroethoxy)aniline (3.4 g, 0.0118 mole) in 40 ml of N-methylpyrrolidinone (NMP). In a separate flask, 3-(2-bromotetrafluoroethoxy)phthalic anhydride (3.0 g, 0.00874 mole) is dissolved in 20 ml of NMP and is added slowly drop wise over 15 minutes to the stirring solution of 4-(2-bromotetrafluoroethoxy)aniline in NMP. The mixture is stirred for 30 minutes at room temperature, after which m-xylene (6 ml) is added and the suspension is heated to 40° C. After heating at 40° C. for 1 hour the is heated to reflux (181° C.) and is refluxed for 6.5 hours to remove water azeotropically. Upon cooling the solvent is removed by evaporation under vacuum and the solid precipitate is recrystallized from dichloromethane/hexane solution (2:1) to provide the product as a light yellow crystalline solid (4.37 g, 81.5 percent yield) with a melting point of 172°-172.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364917
Source datasetuspto-grants-1994_11
ORD IDord-549f028c97de4aecabc90d4b66b73a74
Source noteuspto-grants-1994_11