HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12986252, compound → HCID 12986253, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12986252 | HCID 12986252 | — |
| Reactant | 4-Dimethylamino-4-phenyl-cyclohexylamine | HCID 12986256 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 12986253 | HCID 12986253 | — |
Reaction Steps
4-Dimethylamino-4-phenyl-cyclohexylamine (more polar diastereomer) (218 mg, 1.0 mmole) was added to a solution of (3-phenylpropyl)carbamic acid phenyl ester (255 mg, 1.0 mmole) in dioxane and refluxed for 12 h. Working up was performed by removing the dioxane by distillation and combining the residue with water. The batch was adjusted to pH 11 with 5M NaOH and extracted with ethyl acetate. The organic phase was dried with Na2SO4 and evaporated. The more polar product was obtained as a colorless oil in a yield of 379 mg (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348354B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-5a105e49f4b74e09a2b42dd5f7df8310 |
| Source note | uspto-grants-2008_03 |