HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylsalicylic anhydride → HCID 13051192, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylsalicylic anhydride | HCID 15110 | — |
| Reactant | 1,1'-(Piperazine-1,4-diyl)di(propan-2-ol) | HCID 96698 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13051192 | HCID 13051192 | — |
Reaction Steps
Dissolve acetylsalicylic anhydride (17.1 g; 0.05 moles) in an apolar organic solvent represented for example by ethyl acetate; add 1,4-bis-(2-hydroxypropyl)piperazine (5.06 g; 0.025 moles) to the solution, and heat up to the boiling point until the reaction is completed. After cooling at room temperature, wash the reaction mixture with a 5 percent aqueous solution of potassium carbonate, and then with water. Anhydrify the organic phase (K2CO3), filter, and treat it with anhydrous hydrochloric acid dissolved in diethylether causing by this procedure the precipitation of the raw product that, after collection and drying, can be recrystallized from a low molecular weight alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420482 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-af88a6b3519a486b9b73a9dfb7f6e8f2 |
| Source note | uspto-grants-1983_12 |