HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → HCID 12043587, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-methyl-2-(1-phenyl-vinyl)-phenol | HCID 11074661 | — |
| Product | HCID 12043587 | HCID 12043587 | 82% |
Reaction Steps
0.421 g (2.0 mmole) 4-methyl-2-(1-phenyl-vinyl)-phenol, 0.10 ml (1.15 mmole) morpholine, 6.0 mg (12 μmole) [RhCl(cod)]2 and 10 ml abs. dioxane are agitated in a pressure vessel for 3 days at 120° C. and under a pressure of 90 bar synthesis gas (CO:H2=7.2). Following cooling and relieving of the pressure vessel, the reaction solution undergoes absorptive filtering (eluant: diethylether, then ethanol) through aluminium oxide (activity II-III, basic). Following removal of the solvent, the cleaning of the raw product takes place by column chromatography on silica gel with cyclohexane/MTBE (ratio of volumes=1/1) as the eluant. 255 mg (0.82 mmole, 82%) 4-methyl-2-(3-morpholin-4-yl-1-phenyl-propyl)-phenol are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809225B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-227ea79621964436afdc5f1826554f6c |
| Source note | uspto-grants-2004_10 |