HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-((4-Methoxybenzyl)oxy)isoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | 4-Methoxybenzyl bromide | HCID 165021 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-((4-Methoxybenzyl)oxy)isoindoline-1,3-dione | HCID 717891 | — |
Reaction Steps
To a solution of N-hydroxyphthalimide (11.1 g) and p-methoxybenzyl bromide (13.7 ml) in N,N-dimethylformamide (100 ml) is added triethylamine (6.8 g), and the mixture is stirred at room temperature for 1 hour and at 60° to 70° C. for 1 hour. The reaction mixture is poured into ice water and extracted with ethyl acetate. The extract solution is washed with diluted hydrochloric acid and water, dried and concentrated under reduced pressure. The residue is crystallized from methanol to give N-p-methoxybenzyloxyphthalimide (17 g). mp. 139°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04555578 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-8de6dc04807147e1963b25156eccbd71 |
| Source note | uspto-grants-1985_11 |