HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 9-Benzylamino-7-dodecyl-1,2,3,4-tetrahydroacridine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 9-Chloro-7-dodecyl-1,2,3,4-tetrahydroacridine | HCID 20088989 | — |
| Solvent | Phenol | HCID 996 | — |
| Product | 9-Benzylamino-7-dodecyl-1,2,3,4-tetrahydroacridine hydrochloride | HCID 20089009 | — |
Reaction Steps
9-Chloro-7-dodecyl-1,2,3,4-tetrahydroacridine (2.85 g) was heated at 150° in 60 mL of phenol containing 2.46 g of benzylamine. After 3 hours the reaction mixture was distributed between Et2O and 10% NaOH aqueous solution. The organic phase was washed once more with 10% NaOH, once with H2O, and then treated with 5% HCl. The insoluble hydrochloride was filtered off and recrystallized from isopropanol to give 2.15 g of analytically pure product, mp 194°-195°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05391553 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-4737f658f8a6456386cbf71bd19da64b |
| Source note | uspto-grants-1995_02 |