HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 86600241, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 28351514 | HCID 28351514 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86600241 | HCID 86600241 | — |
Reaction Steps
4-{3-[(3S)-3-methylpiperidin-1-yl]propoxy}aniline was obtained as a light brown oily substance by the method according to Example 18, using 4-nitrophenol and 3-[(3S)-3-methylpiperidin-1-yl]propan-1-ol as starting materials. The obtained oily substance was dissolved in ethyl acetate, 1 Eq of a methanol solution of p-toluenesulfonic acid monohydrate was added, and the target compound was obtained as a light peach-colored solid by filtering off the solid produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07521455B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-99ee335d1d4c4c4383d7c9413cd81d9f |
| Source note | uspto-grants-2009_04 |