HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72325Generated: October 26, 2026
Triethylamine → 3-(4-Benzyloxy-phenyl)-isoxazole-5-carbaldehyde
https://huagongshe.com/reaction/72325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfur trioxide | HCID 24682 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | [3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanol | HCID 64164588 | — |
| Solvent | Dimethylsulfoxide-dichloromethane | HCID 21912085 | — |
| Product | 3-(4-Benzyloxy-phenyl)-isoxazole-5-carbaldehyde | HCID 11818305 | — |
Reaction Steps
[3-(4-benzyloxy-phenyl)-isoxazol-5-yl]-methanol (1.0 g, 3.5 mmol) was dissolved in 60 ml of DMSO/methylene chloride (1:2), to which solution were added dropwise sulfur trioxide.pyridine complex (1.6 g, 10.5 mmol) and triethylamine (2.44 ml, 17.5 mmol), and stirred at 0° C. for about 2 hours. The completion of the reaction was confirmed by TLC, and 10 ml of NH4Cl was added to the solution. The residual solvent was distilled under reduced pressure, and then extracted three times with water and methylene chloride. An organic layer was washed with saline solution. The obtained organic layer was distilled under reduced pressure, followed by column chromatography (ethyl acetate/Hexane=1:2) to obtain 3-(4-benzyloxy-phenyl)-isoxazol-5-carbaldehyde as a desired solid compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828992B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-34655747a0874bf1ba2fad4898e979ab |
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| Source note | uspto-grants-2014_09 |
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