HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1,9b-dihydro-3-isopropyl-3-methyl-5H-imidazo[2,1-a]isoindole2(3H),5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dione | HCID 2729247 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,9b-dihydro-3-isopropyl-3-methyl-5H-imidazo[2,1-a]isoindole2(3H),5-dione | HCID 70621393 | 88.7% |
Reaction Steps
To a stirred suspension of 10.4 g (0.274 mole) sodium borohydride in 164 ml absolute ethanol under nitrogen was added dropwise at 5° C a solution of 133.9 g (0.548 mole) of 2,5-dihydro-3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dione in 155 ml tetrahydrofuran. After the addition, the mixture is stirred a further 3 hours at room temperature and then poured over 1070 g ice with stirring. The mixture is acidified with concentrated HCl and after stirring for 1.5 hours, the precipitate removed by filtration, washed with water and air-dried to give 118.7 g of 1,9b-dihydro-3-isopropyl-3-methyl-5H-imidazo[2,1-a]isoindole2(3H),5-dione, melting point 178°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04092147 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-c60c9ab4aacc4d84a822d526799451b7 |
| Source note | uspto-grants-1978_05 |