HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 86600242, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | 3-Bromo-1-propanol | HCID 12308 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | (2R)-2-methylpyrrolidine hydrobromide | HCID 12444175 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86600242 | HCID 86600242 | — |
Reaction Steps
4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}aniline was obtained as a light brown oily substance by the method according to Example 138, using (2R)-2-methylpyrrolidine hydrobromide, 3-bromopropanol and 4-nitrophenol 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 colorless solid by filtering off the solid produced. (2R)-2-methylpyrrolidine hydrobromide was manufactured by the method described in the literature (J. Org. Chem., 1989, Vol. 54, p. 209)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07521455B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-b8ac1dbdd4444d7986f6c1f19cb47f9e |
| Source note | uspto-grants-2009_04 |