Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329561Generated: October 30, 2026

Phthalic Anhydride → HCID 15051990, compound

https://huagongshe.com/reaction/329561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantHCID 13557219HCID 13557219—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15051990HCID 1505199010.3%

Reaction Steps

This compound was prepared in a manner analogous to that of Example 1, Step C, using 3.0 grams (0.012 mole) of 2-[(4-amino-2-chlorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone and 1.8 grams (0.012 mole) of phthalic anhydride in 125 mL of tetrahydrofuran. The reaction mixture was dissolved in 200 mL of methylene chloride and washed with four 50 mL portions of an aqueous 10% hydrochloric acid solution. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a semi-solid residue. The residue was stirred and heated in ethyl acetate-heptane. The resultant solid was collected by filtration and was recrystallized from acetate/hexane to yield 0.5 gram of 2-[[2-chloro-4-[(2-carboxyphenyl)carbonylamino]phenyl]methyl]-4,4-dimethyl-3-isoxazolidinone; m.p. 172° C., dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892578
Source datasetuspto-grants-1990_01
ORD IDord-7ec9cc5dff5e45279abfbbfd8e6a7dcd
Source noteuspto-grants-1990_01