HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20027815, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(4-Amino-phenyl)-3-propyl-3-aza-bicyclo[3.1.1]heptane-2,4-dione | HCID 14872622 | — |
| Catalyst | Ethanol | HCID 702 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20027815 | HCID 20027815 | — |
Reaction Steps
A solution of 0.11 ml of acetic anhydride in 0.5 ml of tetrahydrofuran is added dropwise to a solution of 260 mg of 1-(4-aminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione and 6 mg of 4-dimethylaminopyridine in 8 ml of tetrahydrofuran. After stirring at room temperature for 21/2 hours, two drops of ethanol are added to the reaction mixture and stirring is continued for a further 15 minutes. After concentration by evaporation and subsequent recrystallisation from ethyl acetate/petroleum ether, the title compound is obtained in the form of white crystals having a melting point of 138.5°-139.5°. Rf (methylene chloride/methanol/glacial acetic acid 40:5:1)=0.55.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857660 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-06aa9c2d2a234e4fb54e5f1470171af4 |
| Source note | uspto-grants-1989_08 |