HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977237Generated: October 30, 2026
p-Toluenesulfonic acid monohydrate → HCID 67707055, compound
https://huagongshe.com/reaction/977237
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 70109253 | HCID 70109253 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67707055 | HCID 67707055 | 77% |
Reaction Steps
A mixture of 5-[2-[4-[1-hydroxy-3-(5-methyl-2-phenyl-4-oxazolyl)propyl]phenyl]ethyl]-2,4-oxazolidinedione (0.32 g), p-toluenesulfonic acid monohydrate (p-TsOH.H2O) (0.145 g) and toluene (40 ml) was stirred under refluxing conditions for 2 hours. The reaction mixture was washed with an aqueous solution of sodium hydrogen carbonate and water, dried (MgSO4) and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography. From the fraction eluted with chloroform-methanol (100:2), 5-[2-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)-1-propenyl]phenyl]ethyl]-2,4-oxazolidinedione (0.235 g, 77%) was obtained, which was then recrystallized from dichloromethane-isopropyl ether to yield colorless needles having a melting point of 175°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614544 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-c66018fd264c4b7fb9aa3f248807c34d |
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| Source note | uspto-grants-1997_03 |
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