HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Hydroxy-2-(4-hydroxyphenyl)-1H-isoindole-1,3(2H)-dione | HCID 19793985 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline-1,3-dione | HCID 69471550 | 186% |
Reaction Steps
To 5-hydroxy-2-(4-hydroxyphenyl)isoindoline-1,3-dione (2.08 g) in DMF (20 mL) was added potassium carbonate (4.62 g) and a solution of benzyl bromide (3.07 g) in DMF (3.0 mL) dropwise under nitrogen atmosphere. The reaction was stirred at room temperature for 2 h then heated to 80° C. for 3 h. The mixture was cooled to room temperature, poured into water (250 mL) and let sit undisturbed for 2.0 h. The white solid was collected by filtration and washed with water. The solid was dried under high vacuum at 50° C. for 18 h yielding the title compound (3.30 g) as a white solid. 1H NMR (DMSO-d6): 7.87 (d, 1H, J=8.4 Hz), 7.48-7.35 (m, 12H), 7.32 (d, 2H, J=8.7 Hz), 7.13 (d, 2H, J=8.7 Hz), 5.35 (s, 2H), 5.17 (s, 2H); MS: 436 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256201B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-e63d17cc269a4f1fbad3885b5a44b3c6 |
| Source note | uspto-grants-2007_08 |