HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → HCID 11287680, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Ethanol hexane | HCID 21879635 | — |
| Reactant | Hexane ethanol diethylamine | HCID 21881120 | — |
| Product | HCID 11287680 | HCID 11287680 | — |
Reaction Steps
R(−) N-(1,2,3,4-tetrahydro-1-naphthalenyl)homopiperazine was obtained as the second material to elute on subjecting racemic material (5.3 g), prepared as in Example 2, to preparative Chiral Pak AD HPLC resolution using a hexane/ethanol mixture with modification with diethylamine. The enantiomeric purity was determined on an analytical scale using hexane:ethanol:diethylamine (90:5:.05, v/v) and detection at 220 nm. The solution containing this enantiomer was concentrated using a rotary evaporator to give the title compound (2.65 g), [α]D22−94° (c=0.64, methanol); 98.5% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06417183B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-57aa50f948cf4bfabfe8a0ce42a1839f |
| Source note | uspto-grants-2002_07 |