HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029909Generated: October 27, 2026
Morpholine → Ethanone, 2-(4-morpholinyl)-1-phenyl-
https://huagongshe.com/reaction/1029909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-Fluoro-1-phenylethan-1-one | HCID 9947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethanone, 2-(4-morpholinyl)-1-phenyl- | HCID 409383 | — |
Reaction Steps
A mixture of 2-fluoroacetophenone (19.9 g), morpholine (21 cc) and potassium carbonate (27.6 g) in dimethyl sulphoxide (32 cc) is heated at 110° C. for 30 hours. The reaction mixture is diluted with water (100 cc) and extracted with ethyl acetate (4×100 cc); the organic solution is washed with distilled water (100 cc), dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a silica gel column (0.04-0.063 mm, diameter 9 cm, height 40 cm), eluting with a mixture of cyclohexane and ethyl acetate (80/20 by volume) and collecting 250 cc fractions. Fraction 24 to 44 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 2-(4-Morpholinyl)acetophenone (4.72 g) is obtained which is used as such for the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102667 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-1f0fbc109ffd44a294702c9d858a21e1 |
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| Source note | uspto-grants-1992_04 |
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