HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Cyclopentyloxy)-4-methoxyaniline → HCID 21994446, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Cyclopentyloxy)-4-methoxyaniline | HCID 2779334 | — |
| Reactant | 2,4-Piperidinedione | HCID 10887863 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21994446 | HCID 21994446 | 100.7% |
Reaction Steps
0.60 g (2.89 mmole) of the 3-cyclopentyloxy-4-methoxyaniline produced in Example 1(2) and 0.33 g (2.89 mmole) of 2, 4-dioxopiperidine were dissolved in solution of 15 ml of benzene, 4 ml of acetonitrile, and 1 ml of methanol and the mixture was stirred at room temperature for 24 hours. After the reaction, the solvent was removed in vacuo and the residue was triturated with ether. The precipitated brown crystal was collected by filtration, then dried in vacuo to obtain the title compound 0.88 g (yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235736B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-1b236d0834ec49dcb7d5354a76e975d7 |
| Source note | uspto-grants-2001_05 |