HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 44276728, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 11957600 | HCID 11957600 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 44276728 | HCID 44276728 | — |
Reaction Steps
The title compound was prepared from (+)-cis-3-((3,5 -bis(trifluoromethyl)phenyl)methyloxy )-2-phenylpiperidine hydrochloride (Example 5) by isolation of the free base (by extraction into ethyl acetate from 10% Na2CO3 solution) and alkylation using a procedure analogous to that described in Example 3, m.p.=40°-42° C.: [α]26D =+149° (c=0.56, MeOH); Found: C, 59.97; H, 4.95; N, 3.36. C21H21NOF6.0.1(H2O) requires C, 60.17; H, 5.10; N, 3.34%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05459270 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-36f25d81644f4ebe89e759288eaae932 |
| Source note | uspto-grants-1995_10 |