HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (Benzo[c][1,2,5]oxadiazol-5-yl)methoxyphthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-(Bromomethyl)-2,1,3-benzoxadiazole | HCID 2735587 | — |
| Product | (Benzo[c][1,2,5]oxadiazol-5-yl)methoxyphthalimide | HCID 66761055 | 94% |
Reaction Steps
5-(Bromomethyl)benzo[c][1,2,5]oxadiazole (0.441 g, 2.07 mmol) was added to a solution of N-hydroxyphthalimide (0.336 g, 2.06 mmol) in dry tetrahydrofuran (15 ml). N,N-Diisopropylethylamine (0.519 g, 4.02 mmol) was added and the solution was stirred at reflux under nitrogen for 23 h and cooled to room temperature. The suspension was concentrated in vacuo to a pale beige solid. This was diluted with water and filtered. The residue was washed with plenty of water and dried under vacuum to give (benzo[c][1,2,5]oxadiazol-5-yl)methoxyphthalimide (0.571 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536157B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-b1be8216ef364d1f9a71013e80cc2570 |
| Source note | uspto-grants-2013_09 |