HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47922Generated: October 25, 2026
Water → 5-(3-Oxo-1-phenylbutyl)-4-phenyl-2-oxo-4-oxazoline
https://huagongshe.com/reaction/47922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 4-Phenyl-3-Buten-2-one | HCID 15909 | — |
| Reactant | 4-Oxazolin-2-one, 4-phenyl- | HCID 118669 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(3-Oxo-1-phenylbutyl)-4-phenyl-2-oxo-4-oxazoline | HCID 15541756 | 86.3% |
Reaction Steps
4-Phenyl-2-oxo-4-oxazoline (1.61 g) and benzalacetone (1.46 g) were dissolved in acetonitrile (20 mL), and methanesulfonic acid (0.96 mL) was added. The obtained mixture was stirred at room temperature for 1 h and water (100 mL) and ethyl acetate (100 mL) were added to the reaction mixture. The organic layer was separated, washed twice with water (50 mL), and concentrated under reduced pressure to give an oily substance. The obtained oily substance was subjected to silica gel column chromatography and eluted with n-hexane-ethyl acetate (1:1). The solvent was evaporated and isopropyl ether (50 mL) was added to the obtained oily substance to allow crystallization and the mixture was stirred at room temperature for 1 h. The crystals were collected by filtration and washed with isopropyl ether (20 mL) to give the title compound (2.65 g; yield 86.3%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699995B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-5040fe76ccd14a1ba39324277a555368 |
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| Source note | uspto-grants-2004_03 |
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