HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenethylamine → HCID 21501142, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenethylamine | HCID 7408 | — |
| Reactant | HCID 20362369 | HCID 20362369 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21501142 | HCID 21501142 | — |
Reaction Steps
A solution of racemic 7-hydroxy-1-nonen-3-one [21.3 g.; crude obtained as in Example 1(d)] in hexane (200 ml.) was treated for 15 hours at 25°C. with a solution of (-)-α-phenylethylamine (11.5 g.) in hexane (115 ml.). The reaction mixture was then purified by chromatography on alumina (660 g.). Elution with hexane first gave unpolar by-products. Hexane-ether-(4:1)-, (1:1), and straight ether then eluted 2-[2-(1-phenylethylamino)-ethyl]-6-ethyl-2-tetrahydropyranol obtained in solid form after evaporation of the solvents.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989724 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-c692dd78d7524766923462af8aad6d45 |
| Source note | uspto-grants-1976_11 |