HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493378Generated: October 30, 2026
Water → 4'-(2-Morpholinoethoxy)acetophenone
https://huagongshe.com/reaction/493378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-(2-Morpholinoethoxy)acetophenone | HCID 30256 | — |
Reaction Steps
Sodium hydride (3.18 g; 0.0795 mol of a powder dispersed at 60%) is added at 23° C. to a solution containing 4-(2-hydroxyethyl)morpholine (9.40 g, 0.072 mol) in dimethylformamide (60 ml). Stirring is maintained for 30 minutes then the compound 4-fluoroacetophenone (5 g, 0.0362 mol) is added. The reaction medium is stirred for one hour at 23° C. then cooled down to 0° C. and water is added. After the addition of ethyl acetate then extraction, the organic phase is washed with a saturated sodium chloride solution, dried over sodium sulphate then the solvent is evaporated off. The residue obtained is adsorbed on silica then purified by chromatography on a Biotage-type silica column (eluent: ethyl acetate-heptane: 6-1). An orange-coloured oil is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534805B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-b80efbc993d04e9fa4f26254d2ce8cc4 |
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| Source note | uspto-grants-2009_05 |
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