HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434516Generated: October 30, 2026
N,N'-Dimethylethylenediamine → 4-(4-Amino-3-fluorophenyl)morpholin-3-one
https://huagongshe.com/reaction/1434516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Morpholinone | HCID 66953 | — |
| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(4-Amino-3-fluorophenyl)morpholin-3-one | HCID 53417798 | — |
Reaction Steps
2.0 g (8.4 mmol) 2-fluoro-4-iodo-aniline, 860 mg (8.5 mmol) morpholin-3-one, 162 mg (0.86 mmol) copper(I)iodide, 2.33 g (16.86 mmol) potassium carbonate and 91 μl N,N′-dimethylethylenediamine are suspended in 18 ml of toluene under an argon atmosphere and stirred for two hours in a microwave at a power of 35 Watts at 140° C. Water is added and the mixture is extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulphate and evaporated to dryness. The residue is purified by chromatography on silica gel (eluant: dichloromethane/methanol 50:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07615549B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-f8d38b09f7904b99ac4181ecc9c58354 |
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| Source note | uspto-grants-2009_11 |
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