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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857548Generated: November 1, 2026

Phthalic Anhydride → HCID 178445559, compound

https://huagongshe.com/reaction/1857548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantHCID 178445560HCID 178445560—
SolventAcetic AcidHCID 176—
ProductHCID 178445559HCID 17844555951%

Reaction Steps

2-[(4-Aminobenzyl)methoxyphosphinoylmethyl]-4-methylpentanoic acid benzyl ester (prepared as described in Example 2/Step A) (242 mg, 0.60 mmole) and phthalic anhydride (133 mg, 0.90 mmole) in acetic acid (10 ml) were refluxed for 1 hour. The cooled reaction mixture was concentrated and the residue dissolved in ethyl acetate (100 ml). This solution was washed with saturated sodium bicarbonate solution (3×20 ml) and dried with magnesium sulfate. Filtration and concentration gave a light yellow oil which was purified by chromatography (ethyl acetate) yielding 162 mg (51%) of 2-{[4-(1,3-dioxo-1,3-dihydroisoindol-2-yl)benzyl]methoxyphosphinoyl methyl}-4-methylpentanoic acid benzyl ester as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147061
Source datasetuspto-grants-2000_11
ORD IDord-3192b73281bd45ffbf357123d6c0a7d2
Source noteuspto-grants-2000_11