HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (1R,2S,5R)-5-Methyl-N-[3-(2-methylphenoxy)propyl]-2-(propan-2-yl)cyclohexane-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Phenoxyethanamine | HCID 15651 | — |
| Reactant | Cyclohexanecarbonyl chloride, 5-methyl-2-(1-methylethyl)- | HCID 13734319 | — |
| Product | (1R,2S,5R)-5-Methyl-N-[3-(2-methylphenoxy)propyl]-2-(propan-2-yl)cyclohexane-1-carboxamide | HCID 67299849 | — |
Reaction Steps
In a 25 mL round bottom flask, fitted with magnetic stirrer, 10 mL of tetrahydrofurane, 6.0 mmol (1.5 eq.) of pyridine and 3.33 mmol of 2-phenoxyethanamine were added. p-Menthane carboxylic acid chloride (4.0 mmol) were added and the mixture was stirred at room temperature for 16 hours, over night. The reaction mixture was extracted with MTBE and HCl (1N in water). The organic layer was washed with NaOH (1N in water), dried over MgSO4 and concentrated. The crude product was purified by column chromatography or crystallized from MtBE and Hexane under dry ice cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377422B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-594f5c5ebda648ef93722bcda216392a |
| Source note | uspto-grants-2013_02 |