HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → ethyl 2-(1,3-dioxoisoindol-2-yl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | NoName_3047 | HCID 69236 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | ethyl 2-(1,3-dioxoisoindol-2-yl)propanoate | HCID 305258 | 89% |
Reaction Steps
20.87 g (0.141 mol) of phthalic anhydride together with 16.5 g (0.141 mol) of ethyl aminopropionate in an open round-bottom flask at 120° C. for 5 h. 300 ml of cyclohexane are added, and the mixture is heated to reflux. The hot cyclohexane solution is decanted off from the remaining oil and completely concentrated. A slowly solidifying viscous oil is obtained (31 g, 89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795278B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-1401872a989446519dd536cd0dce47fe |
| Source note | uspto-grants-2010_09 |