HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977234Generated: November 1, 2026
Trifluoroacetic acid → HCID 11037161, compound
https://huagongshe.com/reaction/977234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 11761871 | HCID 11761871 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11037161 | HCID 11037161 | 82% |
Reaction Steps
A mixture of 5-[3-[4-[1-hydroxy-3-(5-methyl-2-phenyl-4-oxazolyl)propyl]phenyl]propyl]-2,4-oxazolidinedione (0.14 g), triethylsilane [(C2H5)3SiH] (0.075 g) and trifluoroacetic acid (2 ml) was stirred at room temperature for 3 hours. The reaction mixture was poured over water, neutralized with an aqueous solution of sodium hydrogen carbonate and then extracted with ethyl acetate. The ethyl acetate layer was washed with 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 (100:3), 5-[3-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propyl]phenyl]propyl]-2,4-oxazolidinedione (0.11 g, 82%) was obtained, which was then recrystallized from ether-methanol to yield colorless needles having a melting point of 119°-120° 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-80a8f4829fe64243a57c3bbb819a9d02 |
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| Source note | uspto-grants-1997_03 |
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