HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Hydroxyphthalimide → 2-(3-Methoxy-4-pent-2-ynyloxy-benzyloxy)-isoindole-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Chloromethyl-2-methoxy-1-pent-2-ynyloxy-benzene | HCID 18442093 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-Methoxy-4-pent-2-ynyloxy-benzyloxy)-isoindole-1,3-dione | HCID 18442091 | — |
Reaction Steps
4-Chloromethyl-2-methoxy-1-pent-2-ynyloxy-benzene (28 g, 0.12 mol) and N-hydroxyphthalimide (19.5 g, 0.12 mol) are dissolved in 180 ml of N,N-dimethylformamide. The reaction mixture is heated to +70° C. and potassium hydroxide (24 ml of a 5 M solution in methanol, 0.12 mol) is added at this temperature. The reaction is stirred for 1 hour at +70° C., subsequently cooled to room temperature and poured on water. This mixture is stirred for one further hour and filtered. The resulting crystalls are washed with water and recrystallized from methanol/acetone (8:1) to yield 2-(3-methoxy-4-pent-2-ynyloxy-benzyloxy)-isoindole-1,3-dione as colourless crystalls.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189873B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-4357ef393f964306862bd9846e1d81b5 |
| Source note | uspto-grants-2007_03 |