HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalaldehyde → 2-(4-acetylphenyl)isoindolin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalaldehyde | HCID 4807 | — |
| Reactant | 4-Acetylphenyl isocyanate | HCID 99452 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-acetylphenyl)isoindolin-1-one | HCID 910849 | 42.6% |
Reaction Steps
A mixture of 4-acetylphenylisocyanate (27.5 g, 0.17 mol) and o-phthalicdicarboxaldehyde (25.0 g, 0.186 mol) is heated in an oil bath at 170°-175° C. for 4.0 hours under nitrogen atmosphere. On cooling the melt solidified which is pulverized and refluxed with CH2Cl2 and CH30H and filtered to give 18.2 g (41.4%) of the desired 2-(4-acetylphenyl)-2,3-dihydro-lH-isoindole-1-one, mp 235°-237° C. The residue is recrystallized from DMF (1800 ml). Yield 13.0 g (29.6%), mp 236°-239° C. (Jap. patent J5 7050-960; mp 243°-244° C. for the nonsolvated compound, prepared by a different route).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075330 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-feb0e4fac67d4bb2875429e3238b6001 |
| Source note | uspto-grants-1991_12 |