HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 178445559, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | HCID 178445560 | HCID 178445560 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178445559 | HCID 178445559 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06147061 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-3192b73281bd45ffbf357123d6c0a7d2 |
| Source note | uspto-grants-2000_11 |