HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-bromo-1,1-dimethoxypentane → 2-(5,5-Dimethoxypentyl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-bromo-1,1-dimethoxypentane | HCID 11074684 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(5,5-Dimethoxypentyl)-1H-isoindole-1,3(2H)-dione | HCID 13286118 | — |
Reaction Steps
A mixture of potassium phthalimide (0.48 g) and 5-bromopentanal dimethyl acetal (0.50 g) in dry dimethylformamide (3 ml) was stirred at 90° for 5 h and then allowed to cool. The resultant yellow suspension was then partitioned between water (30 ml) and ethyl acetate (3×30 ml). The combined organic extracts were then dried (Na2SO4) and concentrated in vauco.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816470 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-7b14b9fab9fc426eb1278cc5b0f1bd6e |
| Source note | uspto-grants-1989_03 |