HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(4-Biphenylyl)-2-(4-morpholinyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(1,1'-Biphenyl)-4-yl-2-bromoethanone | HCID 67282 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Biphenylyl)-2-(4-morpholinyl)ethanone | HCID 57418661 | 93.7% |
Reaction Steps
Morpholine (1.67 g, 19.1 mmol) in anhydrous ether (20 mL) was added dropwise to a solution of 1-(4-biphenylyl)-2-bromoethanone (2.63 g, 9.56 mmol) and triethylamine (TEA) (2.90 g, 28.68 mmol) in anhydrous ether (50 mL) at 0° C. over 30 min. The reaction mixture was then warmed to room temperature. After stirring for 2 h, water (80 mL) was added and the aqueous layer was extracted with ethyl acetate (2×60 mL). The combined organic layer was dried over MgSO4 and concentrated to yield the title compound as a light yellow solid (2.52 g, 93%), which was used without further purification. MS (ES) m/e 281[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432258B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-ee817ef9525149bd9242d480d5fbc11c |
| Source note | uspto-grants-2008_10 |